Canonical Allele Identifier: CA376997715

Gene: ANK3

Linked Data

• MyVariant Identifiers: chr10:g.61829546C>G (hg19) ; chr10:g.60069788C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60069788C>G , CM000672.2:g.60069788C>G	GRCh38
NC_000010.10:g.61829546C>G , CM000672.1:g.61829546C>G	GRCh37
NC_000010.9:g.61499552C>G	NCBI36
NG_029917.1:g.668739G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467420.7:c.4490-1779G>C	ENSP00000423968.2:n.4490-1779G>C
ENST00000503366.6:c.4409-1779G>C	ENSP00000425236.1:n.4409-1779G>C
ENST00000280772.7:c.11093G>C MANE Select	ENSP00000280772.1:p.Ser3698Thr
ENST00000280772.6:c.11093G>C	ENSP00000280772.1:p.Ser3698Thr
ENST00000355288.6:c.1808-1779G>C	ENSP00000347436.2:n.1808-1779G>C
ENST00000373820.5:c.182-1779G>C	ENSP00000362926.1:n.182-1779G>C
ENST00000373827.6:c.4388-1779G>C	ENSP00000362933.2:n.4388-1779G>C
ENST00000503366.5:c.4409-1779G>C	ENSP00000425236.1:n.4409-1779G>C
ENST00000511043.5:c.85-1779G>C
ENST00000610321.4:c.4041-1779G>C
ENST00000610901.4:c.486+190G>C
ENST00000613207.4:c.306+190G>C
ENST00000616444.4:c.1224-1779G>C
ENST00000618374.4:c.1808-1779G>C	ENSP00000479018.1:n.1808-1779G>C
ENST00000621739.1:c.2592+190G>C
NM_001149.3:c.1808-1779G>C	NP_001140.2:n.1808-1779G>C
NM_001204403.1:c.4388-1779G>C	NP_001191332.1:n.4388-1779G>C
NM_001204404.1:c.4409-1779G>C	NP_001191333.1:n.4409-1779G>C
NM_020987.3:c.11093G>C	NP_066267.2:p.Ser3698Thr
XM_005269715.2:c.4460-1779G>C	XP_005269772.1:n.4460-1779G>C
XM_005269716.2:c.4406-1779G>C	XP_005269773.1:n.4406-1779G>C
XM_006717791.2:c.7082-1779G>C	XP_006717854.1:n.7082-1779G>C
XM_006717793.2:c.7082-1779G>C	XP_006717856.1:n.7082-1779G>C
XM_006717795.2:c.7082-1779G>C	XP_006717858.1:n.7082-1779G>C
XM_006717796.2:c.7082-1779G>C	XP_006717859.1:n.7082-1779G>C
XM_006717802.2:c.4499-1779G>C	XP_006717865.1:n.4499-1779G>C
XM_011539700.1:c.7070-1779G>C	XP_011538002.1:n.7070-1779G>C
XM_011539701.1:c.7064-1779G>C	XP_011538003.1:n.7064-1779G>C
XM_011539702.1:c.7025-1779G>C	XP_011538004.1:n.7025-1779G>C
XM_011539703.1:c.7004-1779G>C	XP_011538005.1:n.7004-1779G>C
XM_011539704.1:c.6983-1779G>C	XP_011538006.1:n.6983-1779G>C
XM_011539705.1:c.6983-1779G>C	XP_011538007.1:n.6983-1779G>C
XM_011539706.1:c.6971-1779G>C	XP_011538008.1:n.6971-1779G>C
XM_011539707.1:c.7082-1779G>C	XP_011538009.1:n.7082-1779G>C
XM_011539708.1:c.7082-1779G>C	XP_011538010.1:n.7082-1779G>C
XM_011539709.1:c.7082-1779G>C	XP_011538011.1:n.7082-1779G>C
XM_011539710.1:c.4499-1779G>C	XP_011538012.1:n.4499-1779G>C
XM_011539711.1:c.4472-1779G>C	XP_011538013.1:n.4472-1779G>C
XM_011539712.1:c.4463-1779G>C	XP_011538014.1:n.4463-1779G>C
XM_011539713.1:c.4436-1779G>C	XP_011538015.1:n.4436-1779G>C
XM_011539714.1:c.4430-1779G>C	XP_011538016.1:n.4430-1779G>C
XM_011539715.1:c.4418-1779G>C	XP_011538017.1:n.4418-1779G>C
XM_011539716.1:c.4472-1779G>C	XP_011538018.1:n.4472-1779G>C
XM_011539717.1:c.4460-1779G>C	XP_011538019.1:n.4460-1779G>C
XM_011539718.1:c.4343-1779G>C	XP_011538020.1:n.4343-1779G>C
NM_001320874.1:c.4406-1779G>C	NP_001307803.1:n.4406-1779G>C
NM_020987.4:c.11093G>C	NP_066267.2:p.Ser3698Thr
XM_005269715.3:c.4460-1779G>C	XP_005269772.1:n.4460-1779G>C
XM_006717796.3:c.7082-1779G>C	XP_006717859.1:n.7082-1779G>C
XM_006717802.3:c.4499-1779G>C	XP_006717865.1:n.4499-1779G>C
XM_011539708.2:c.7082-1779G>C	XP_011538010.1:n.7082-1779G>C
XM_011539709.2:c.7082-1779G>C	XP_011538011.1:n.7082-1779G>C
XM_017016110.1:c.11165G>C	XP_016871599.1:p.Ser3722Thr
XM_017016111.1:c.11153G>C	XP_016871600.1:p.Ser3718Thr
XM_017016112.1:c.11150G>C	XP_016871601.1:p.Ser3717Thr
XM_017016113.1:c.11138G>C	XP_016871602.1:p.Ser3713Thr
XM_017016114.1:c.11114G>C	XP_016871603.1:p.Ser3705Thr
XM_017016115.1:c.11087G>C	XP_016871604.1:p.Ser3696Thr
XM_017016116.1:c.11165G>C	XP_016871605.1:p.Ser3722Thr
XM_017016117.1:c.11165G>C	XP_016871606.1:p.Ser3722Thr
XM_017016118.1:c.10975+190G>C	XP_016871607.1:n.10975+190G>C
XM_017016119.1:c.10975+190G>C	XP_016871608.1:n.10975+190G>C
XM_017016120.1:c.10975+190G>C	XP_016871609.1:n.10975+190G>C
XM_017016121.1:c.10948+190G>C	XP_016871610.1:n.10948+190G>C
XM_017016122.1:c.6989-1779G>C	XP_016871611.1:n.6989-1779G>C
XM_017016123.1:c.7082-1779G>C	XP_016871612.1:n.7082-1779G>C
XM_017016124.1:c.7055-1779G>C	XP_016871613.1:n.7055-1779G>C
XM_017016125.1:c.7055-1779G>C	XP_016871614.1:n.7055-1779G>C
XM_017016126.1:c.6950-1779G>C	XP_016871615.1:n.6950-1779G>C
XM_017016127.1:c.6923-1779G>C	XP_016871616.1:n.6923-1779G>C
XM_017016128.1:c.4472-1779G>C	XP_016871617.1:n.4472-1779G>C
XM_017016129.1:c.4472-1779G>C	XP_016871618.1:n.4472-1779G>C
XM_017016130.1:c.4406-1779G>C	XP_016871619.1:n.4406-1779G>C
XM_017016131.1:c.4391-1779G>C	XP_016871620.1:n.4391-1779G>C
XM_017016132.1:c.4370-1779G>C	XP_016871621.1:n.4370-1779G>C
XM_017016134.1:c.4340-1779G>C	XP_016871623.1:n.4340-1779G>C
XM_017016136.1:c.4499-1779G>C	XP_016871625.1:n.4499-1779G>C
XM_017016137.1:c.4472-1779G>C	XP_016871626.1:n.4472-1779G>C
XM_017016138.1:c.4472-1779G>C	XP_016871627.1:n.4472-1779G>C
XM_017016141.1:c.4367-1779G>C	XP_016871630.1:n.4367-1779G>C
XM_024447953.1:c.11138G>C	XP_024303721.1:p.Ser3713Thr
XM_024447954.1:c.11111G>C	XP_024303722.1:p.Ser3704Thr
XM_024447955.1:c.11102G>C	XP_024303723.1:p.Ser3701Thr
XM_024447956.1:c.11099G>C	XP_024303724.1:p.Ser3700Thr
XM_024447957.1:c.11066G>C	XP_024303725.1:p.Ser3689Thr
XM_024447958.1:c.11048G>C	XP_024303726.1:p.Ser3683Thr
XM_024447959.1:c.11048G>C	XP_024303727.1:p.Ser3683Thr
XM_024447960.1:c.11036G>C	XP_024303728.1:p.Ser3679Thr
XM_024447961.1:c.11033G>C	XP_024303729.1:p.Ser3678Thr
XM_024447962.1:c.10948+190G>C	XP_024303730.1:n.10948+190G>C
XM_024447963.1:c.7082-1779G>C	XP_024303731.1:n.7082-1779G>C
XM_024447964.1:c.4436-1779G>C	XP_024303732.1:n.4436-1779G>C
XM_024447965.1:c.4463-1779G>C	XP_024303733.1:n.4463-1779G>C
NM_020987.5:c.11093G>C MANE Select	NP_066267.2:p.Ser3698Thr
NM_001204403.2:c.4388-1779G>C	NP_001191332.1:n.4388-1779G>C
NM_001204404.2:c.4409-1779G>C	NP_001191333.1:n.4409-1779G>C
NM_001320874.2:c.4406-1779G>C	NP_001307803.1:n.4406-1779G>C
NM_001149.4:c.1808-1779G>C	NP_001140.2:n.1808-1779G>C