Canonical Allele Identifier: CA1913750256
Gene: ANK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60071495C= , CM000672.2:g.60071495C= GRCh38
NC_000010.10:g.61831253C= , CM000672.1:g.61831253C= GRCh37
NC_000010.9:g.61501259C= NCBI36
NG_029917.1:g.667032G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000467420.7:c.4490-3486G= ENSP00000423968.2:n.4490-3486G=
ENST00000503366.6:c.4409-3486G= ENSP00000425236.1:n.4409-3486G=
ENST00000280772.7:c.9386G= MANE Select ENSP00000280772.1:p.Arg3129=
ENST00000280772.6:c.9386G= ENSP00000280772.1:p.Arg3129=
ENST00000355288.6:c.1808-3486G= ENSP00000347436.2:n.1808-3486G=
ENST00000373820.5:c.182-3486G= ENSP00000362926.1:n.182-3486G=
ENST00000373827.6:c.4388-3486G= ENSP00000362933.2:n.4388-3486G=
ENST00000503366.5:c.4409-3486G= ENSP00000425236.1:n.4409-3486G=
ENST00000511043.5:c.85-3486G=
ENST00000610321.4:c.4040+2377G=
ENST00000616444.4:c.1224-3486G=
ENST00000618374.4:c.1808-3486G= ENSP00000479018.1:n.1808-3486G=
ENST00000621739.1:c.1075G=
NM_001149.3:c.1808-3486G= NP_001140.2:n.1808-3486G=
NM_001204403.1:c.4388-3486G= NP_001191332.1:n.4388-3486G=
NM_001204404.1:c.4409-3486G= NP_001191333.1:n.4409-3486G=
NM_020987.3:c.9386G= NP_066267.2:p.Arg3129=
XM_005269715.2:c.4460-3486G= XP_005269772.1:n.4460-3486G=
XM_005269716.2:c.4406-3486G= XP_005269773.1:n.4406-3486G=
XM_006717791.2:c.7081+2377G= XP_006717854.1:n.7081+2377G=
XM_006717793.2:c.7081+2377G= XP_006717856.1:n.7081+2377G=
XM_006717795.2:c.7081+2377G= XP_006717858.1:n.7081+2377G=
XM_006717796.2:c.7081+2377G= XP_006717859.1:n.7081+2377G=
XM_006717802.2:c.4499-3486G= XP_006717865.1:n.4499-3486G=
XM_011539700.1:c.7069+2377G= XP_011538002.1:n.7069+2377G=
XM_011539701.1:c.7063+2377G= XP_011538003.1:n.7063+2377G=
XM_011539702.1:c.7024+2377G= XP_011538004.1:n.7024+2377G=
XM_011539703.1:c.7003+2377G= XP_011538005.1:n.7003+2377G=
XM_011539704.1:c.6982+2377G= XP_011538006.1:n.6982+2377G=
XM_011539705.1:c.6982+2377G= XP_011538007.1:n.6982+2377G=
XM_011539706.1:c.6970+2377G= XP_011538008.1:n.6970+2377G=
XM_011539707.1:c.7081+2377G= XP_011538009.1:n.7081+2377G=
XM_011539708.1:c.7081+2377G= XP_011538010.1:n.7081+2377G=
XM_011539709.1:c.7081+2377G= XP_011538011.1:n.7081+2377G=
XM_011539710.1:c.4499-3486G= XP_011538012.1:n.4499-3486G=
XM_011539711.1:c.4472-3486G= XP_011538013.1:n.4472-3486G=
XM_011539712.1:c.4463-3486G= XP_011538014.1:n.4463-3486G=
XM_011539713.1:c.4436-3486G= XP_011538015.1:n.4436-3486G=
XM_011539714.1:c.4429+2377G= XP_011538016.1:n.4429+2377G=
XM_011539715.1:c.4417+2377G= XP_011538017.1:n.4417+2377G=
XM_011539716.1:c.4472-3486G= XP_011538018.1:n.4472-3486G=
XM_011539717.1:c.4460-3486G= XP_011538019.1:n.4460-3486G=
XM_011539718.1:c.4343-3486G= XP_011538020.1:n.4343-3486G=
NM_001320874.1:c.4406-3486G= NP_001307803.1:n.4406-3486G=
NM_020987.4:c.9386G= NP_066267.2:p.Arg3129=
XM_005269715.3:c.4460-3486G= XP_005269772.1:n.4460-3486G=
XM_006717796.3:c.7081+2377G= XP_006717859.1:n.7081+2377G=
XM_006717802.3:c.4499-3486G= XP_006717865.1:n.4499-3486G=
XM_011539708.2:c.7081+2377G= XP_011538010.1:n.7081+2377G=
XM_011539709.2:c.7081+2377G= XP_011538011.1:n.7081+2377G=
XM_017016110.1:c.9458G= XP_016871599.1:p.Arg3153=
XM_017016111.1:c.9446G= XP_016871600.1:p.Arg3149=
XM_017016112.1:c.9443G= XP_016871601.1:p.Arg3148=
XM_017016113.1:c.9431G= XP_016871602.1:p.Arg3144=
XM_017016114.1:c.9407G= XP_016871603.1:p.Arg3136=
XM_017016115.1:c.9380G= XP_016871604.1:p.Arg3127=
XM_017016116.1:c.9458G= XP_016871605.1:p.Arg3153=
XM_017016117.1:c.9458G= XP_016871606.1:p.Arg3153=
XM_017016118.1:c.9458G= XP_016871607.1:p.Arg3153=
XM_017016119.1:c.9458G= XP_016871608.1:p.Arg3153=
XM_017016120.1:c.9458G= XP_016871609.1:p.Arg3153=
XM_017016121.1:c.9431G= XP_016871610.1:p.Arg3144=
XM_017016122.1:c.6988+2377G= XP_016871611.1:n.6988+2377G=
XM_017016123.1:c.7081+2377G= XP_016871612.1:n.7081+2377G=
XM_017016124.1:c.7054+2377G= XP_016871613.1:n.7054+2377G=
XM_017016125.1:c.7054+2377G= XP_016871614.1:n.7054+2377G=
XM_017016126.1:c.6949+2377G= XP_016871615.1:n.6949+2377G=
XM_017016127.1:c.6922+2377G= XP_016871616.1:n.6922+2377G=
XM_017016128.1:c.4472-3486G= XP_016871617.1:n.4472-3486G=
XM_017016129.1:c.4472-3486G= XP_016871618.1:n.4472-3486G=
XM_017016130.1:c.4406-3486G= XP_016871619.1:n.4406-3486G=
XM_017016131.1:c.4391-3486G= XP_016871620.1:n.4391-3486G=
XM_017016132.1:c.4370-3486G= XP_016871621.1:n.4370-3486G=
XM_017016134.1:c.4340-3486G= XP_016871623.1:n.4340-3486G=
XM_017016136.1:c.4499-3486G= XP_016871625.1:n.4499-3486G=
XM_017016137.1:c.4472-3486G= XP_016871626.1:n.4472-3486G=
XM_017016138.1:c.4472-3486G= XP_016871627.1:n.4472-3486G=
XM_017016141.1:c.4367-3486G= XP_016871630.1:n.4367-3486G=
XM_024447953.1:c.9431G= XP_024303721.1:p.Arg3144=
XM_024447954.1:c.9404G= XP_024303722.1:p.Arg3135=
XM_024447955.1:c.9395G= XP_024303723.1:p.Arg3132=
XM_024447956.1:c.9392G= XP_024303724.1:p.Arg3131=
XM_024447957.1:c.9359G= XP_024303725.1:p.Arg3120=
XM_024447958.1:c.9341G= XP_024303726.1:p.Arg3114=
XM_024447959.1:c.9341G= XP_024303727.1:p.Arg3114=
XM_024447960.1:c.9329G= XP_024303728.1:p.Arg3110=
XM_024447961.1:c.9326G= XP_024303729.1:p.Arg3109=
XM_024447962.1:c.9431G= XP_024303730.1:p.Arg3144=
XM_024447963.1:c.7081+2377G= XP_024303731.1:n.7081+2377G=
XM_024447964.1:c.4436-3486G= XP_024303732.1:n.4436-3486G=
XM_024447965.1:c.4463-3486G= XP_024303733.1:n.4463-3486G=
NM_020987.5:c.9386G= MANE Select NP_066267.2:p.Arg3129=
NM_001204403.2:c.4388-3486G= NP_001191332.1:n.4388-3486G=
NM_001204404.2:c.4409-3486G= NP_001191333.1:n.4409-3486G=
NM_001320874.2:c.4406-3486G= NP_001307803.1:n.4406-3486G=
NM_001149.4:c.1808-3486G= NP_001140.2:n.1808-3486G=