Canonical Allele Identifier: CA5510869
Gene: ANK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60063186T>C , CM000672.2:g.60063186T>C GRCh38
NC_000010.10:g.61822944T>C , CM000672.1:g.61822944T>C GRCh37
NC_000010.9:g.61492950T>C NCBI36
NG_029917.1:g.675341A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000467420.7:c.4765A>G ENSP00000423968.2:p.Ile1589Val
ENST00000503366.6:c.4684A>G ENSP00000425236.1:p.Ile1562Val
ENST00000280772.7:c.12520A>G MANE Select ENSP00000280772.1:p.Ile4174Val
ENST00000280772.6:c.12520A>G ENSP00000280772.1:p.Ile4174Val
ENST00000355288.6:c.2083A>G ENSP00000347436.2:p.Ile695Val
ENST00000373820.5:c.457A>G ENSP00000362926.1:p.Ile153Val
ENST00000373827.6:c.4663A>G ENSP00000362933.2:p.Ile1555Val
ENST00000459732.2:c.201A>G
ENST00000503366.5:c.4684A>G ENSP00000425236.1:p.Ile1562Val
ENST00000511043.5:c.360A>G
ENST00000514197.5:c.201A>G
ENST00000610321.4:c.4316A>G
ENST00000610901.4:c.762A>G
ENST00000613207.4:c.582A>G
ENST00000616444.4:c.1499A>G
ENST00000618374.4:c.2083A>G ENSP00000479018.1:p.Ile695Val
ENST00000621739.1:c.3089A>G
NM_001149.3:c.2083A>G NP_001140.2:p.Ile695Val
NM_001204403.1:c.4663A>G NP_001191332.1:p.Ile1555Val
NM_001204404.1:c.4684A>G NP_001191333.1:p.Ile1562Val
NM_020987.3:c.12520A>G NP_066267.2:p.Ile4174Val
XM_005269715.2:c.4735A>G XP_005269772.1:p.Ile1579Val
XM_005269716.2:c.4681A>G XP_005269773.1:p.Ile1561Val
XM_006717791.2:c.7357A>G XP_006717854.1:p.Ile2453Val
XM_006717793.2:c.7357A>G XP_006717856.1:p.Ile2453Val
XM_006717795.2:c.7357A>G XP_006717858.1:p.Ile2453Val
XM_006717796.2:c.7357A>G XP_006717859.1:p.Ile2453Val
XM_006717802.2:c.4774A>G XP_006717865.1:p.Ile1592Val
XM_011539700.1:c.7345A>G XP_011538002.1:p.Ile2449Val
XM_011539701.1:c.7339A>G XP_011538003.1:p.Ile2447Val
XM_011539702.1:c.7300A>G XP_011538004.1:p.Ile2434Val
XM_011539703.1:c.7279A>G XP_011538005.1:p.Ile2427Val
XM_011539704.1:c.7258A>G XP_011538006.1:p.Ile2420Val
XM_011539705.1:c.7258A>G XP_011538007.1:p.Ile2420Val
XM_011539706.1:c.7246A>G XP_011538008.1:p.Ile2416Val
XM_011539707.1:c.7357A>G XP_011538009.1:p.Ile2453Val
XM_011539708.1:c.7357A>G XP_011538010.1:p.Ile2453Val
XM_011539709.1:c.7357A>G XP_011538011.1:p.Ile2453Val
XM_011539710.1:c.4774A>G XP_011538012.1:p.Ile1592Val
XM_011539711.1:c.4747A>G XP_011538013.1:p.Ile1583Val
XM_011539712.1:c.4738A>G XP_011538014.1:p.Ile1580Val
XM_011539713.1:c.4711A>G XP_011538015.1:p.Ile1571Val
XM_011539714.1:c.4705A>G XP_011538016.1:p.Ile1569Val
XM_011539715.1:c.4693A>G XP_011538017.1:p.Ile1565Val
XM_011539716.1:c.4747A>G XP_011538018.1:p.Ile1583Val
XM_011539717.1:c.4735A>G XP_011538019.1:p.Ile1579Val
XM_011539718.1:c.4618A>G XP_011538020.1:p.Ile1540Val
NM_001320874.1:c.4681A>G NP_001307803.1:p.Ile1561Val
NM_020987.4:c.12520A>G NP_066267.2:p.Ile4174Val
XM_005269715.3:c.4735A>G XP_005269772.1:p.Ile1579Val
XM_006717796.3:c.7357A>G XP_006717859.1:p.Ile2453Val
XM_006717802.3:c.4774A>G XP_006717865.1:p.Ile1592Val
XM_011539708.2:c.7357A>G XP_011538010.1:p.Ile2453Val
XM_011539709.2:c.7357A>G XP_011538011.1:p.Ile2453Val
XM_017016110.1:c.12592A>G XP_016871599.1:p.Ile4198Val
XM_017016111.1:c.12580A>G XP_016871600.1:p.Ile4194Val
XM_017016112.1:c.12577A>G XP_016871601.1:p.Ile4193Val
XM_017016113.1:c.12565A>G XP_016871602.1:p.Ile4189Val
XM_017016114.1:c.12541A>G XP_016871603.1:p.Ile4181Val
XM_017016115.1:c.12514A>G XP_016871604.1:p.Ile4172Val
XM_017016116.1:c.12592A>G XP_016871605.1:p.Ile4198Val
XM_017016117.1:c.12592A>G XP_016871606.1:p.Ile4198Val
XM_017016118.1:c.11251A>G XP_016871607.1:p.Ile3751Val
XM_017016119.1:c.11251A>G XP_016871608.1:p.Ile3751Val
XM_017016120.1:c.11251A>G XP_016871609.1:p.Ile3751Val
XM_017016121.1:c.11224A>G XP_016871610.1:p.Ile3742Val
XM_017016122.1:c.7264A>G XP_016871611.1:p.Ile2422Val
XM_017016123.1:c.7357A>G XP_016871612.1:p.Ile2453Val
XM_017016124.1:c.7330A>G XP_016871613.1:p.Ile2444Val
XM_017016125.1:c.7330A>G XP_016871614.1:p.Ile2444Val
XM_017016126.1:c.7225A>G XP_016871615.1:p.Ile2409Val
XM_017016127.1:c.7198A>G XP_016871616.1:p.Ile2400Val
XM_017016128.1:c.4747A>G XP_016871617.1:p.Ile1583Val
XM_017016129.1:c.4747A>G XP_016871618.1:p.Ile1583Val
XM_017016130.1:c.4681A>G XP_016871619.1:p.Ile1561Val
XM_017016131.1:c.4666A>G XP_016871620.1:p.Ile1556Val
XM_017016132.1:c.4645A>G XP_016871621.1:p.Ile1549Val
XM_017016134.1:c.4615A>G XP_016871623.1:p.Ile1539Val
XM_017016136.1:c.4774A>G XP_016871625.1:p.Ile1592Val
XM_017016137.1:c.4747A>G XP_016871626.1:p.Ile1583Val
XM_017016138.1:c.4747A>G XP_016871627.1:p.Ile1583Val
XM_017016141.1:c.4642A>G XP_016871630.1:p.Ile1548Val
XM_024447953.1:c.12565A>G XP_024303721.1:p.Ile4189Val
XM_024447954.1:c.12538A>G XP_024303722.1:p.Ile4180Val
XM_024447955.1:c.12529A>G XP_024303723.1:p.Ile4177Val
XM_024447956.1:c.12526A>G XP_024303724.1:p.Ile4176Val
XM_024447957.1:c.12493A>G XP_024303725.1:p.Ile4165Val
XM_024447958.1:c.12475A>G XP_024303726.1:p.Ile4159Val
XM_024447959.1:c.12475A>G XP_024303727.1:p.Ile4159Val
XM_024447960.1:c.12463A>G XP_024303728.1:p.Ile4155Val
XM_024447961.1:c.12460A>G XP_024303729.1:p.Ile4154Val
XM_024447962.1:c.11224A>G XP_024303730.1:p.Ile3742Val
XM_024447963.1:c.7357A>G XP_024303731.1:p.Ile2453Val
XM_024447964.1:c.4711A>G XP_024303732.1:p.Ile1571Val
XM_024447965.1:c.4738A>G XP_024303733.1:p.Ile1580Val
NM_020987.5:c.12520A>G MANE Select NP_066267.2:p.Ile4174Val
NM_001204403.2:c.4663A>G NP_001191332.1:p.Ile1555Val
NM_001204404.2:c.4684A>G NP_001191333.1:p.Ile1562Val
NM_001320874.2:c.4681A>G NP_001307803.1:p.Ile1561Val
NM_001149.4:c.2083A>G NP_001140.2:p.Ile695Val