Canonical Allele Identifier: CA1779071195
Gene: ANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41668427C= , CM000670.2:g.41668427C= GRCh38
NC_000008.10:g.41525945C= , CM000670.1:g.41525945C= GRCh37
NC_000008.9:g.41645102C= NCBI36
NG_012820.1:g.233336G=
NG_012820.2:g.233336G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265709.14:c.5357G= ENSP00000265709.8:p.Gly1786=
ENST00000705521.1:c.5453G= ENSP00000516136.1:p.Gly1818=
ENST00000705522.1:c.5270G= ENSP00000516137.1:p.Gly1757=
ENST00000265709.13:c.5357G= ENSP00000265709.8:p.Gly1786=
ENST00000289734.13:c.5234G= MANE Select ENSP00000289734.8:p.Gly1745=
ENST00000645531.1:c.1248G=
ENST00000265709.12:c.5357G= ENSP00000265709.8:p.Gly1786=
ENST00000289734.11:c.5234G= ENSP00000289734.7:p.Gly1745=
ENST00000347528.8:c.5234G= ENSP00000339620.4:p.Gly1745=
ENST00000518061.1:c.806G=
ENST00000520299.5:c.2712G=
ENST00000524227.5:n.2628G=
NM_000037.3:c.5234G= NP_000028.3:p.Gly1745=
NM_001142446.1:c.5357G= NP_001135918.1:p.Gly1786=
NM_020475.2:c.5234G= NP_065208.2:p.Gly1745=
NM_020476.2:c.5234G= NP_065209.2:p.Gly1745=
NM_020477.2:c.4748G= NP_065210.2:p.Gly1583=
XM_005273476.3:c.5357G= XP_005273533.1:p.Gly1786=
XM_011544490.1:c.5498G= XP_011542792.1:p.Gly1833=
XM_011544491.1:c.5498G= XP_011542793.1:p.Gly1833=
XM_011544492.1:c.5399G= XP_011542794.1:p.Gly1800=
XM_011544493.1:c.5498G= XP_011542795.1:p.Gly1833=
XM_011544494.1:c.5453G= XP_011542796.1:p.Gly1818=
XM_011544495.1:c.5453G= XP_011542797.1:p.Gly1818=
XM_011544496.1:c.5498G= XP_011542798.1:p.Gly1833=
XM_011544497.1:c.5333G= XP_011542799.1:p.Gly1778=
XM_011544498.1:c.5315G= XP_011542800.1:p.Gly1772=
XM_011544499.1:c.5498G= XP_011542801.1:p.Gly1833=
XM_011544500.1:c.5333G= XP_011542802.1:p.Gly1778=
XM_011544501.1:c.5333G= XP_011542803.1:p.Gly1778=
XM_011544502.1:c.5333G= XP_011542804.1:p.Gly1778=
XM_011544503.1:c.4967G= XP_011542805.1:p.Gly1656=
XM_011544504.1:c.4847G= XP_011542806.1:p.Gly1616=
XM_011544505.1:c.4847G= XP_011542807.1:p.Gly1616=
XM_011544506.1:c.*15G= XP_011542808.1:n.*15G=
XR_949389.1:n.5089G=
XM_005273476.4:c.5357G= XP_005273533.1:p.Gly1786=
XM_011544490.3:c.5498G= XP_011542792.1:p.Gly1833=
XM_011544491.3:c.5498G= XP_011542793.1:p.Gly1833=
XM_011544494.3:c.5453G= XP_011542796.1:p.Gly1818=
XM_011544495.3:c.5453G= XP_011542797.1:p.Gly1818=
XM_011544496.3:c.5498G= XP_011542798.1:p.Gly1833=
XM_011544500.2:c.5333G= XP_011542802.1:p.Gly1778=
XM_011544501.2:c.5333G= XP_011542803.1:p.Gly1778=
XM_011544502.2:c.5333G= XP_011542804.1:p.Gly1778=
XM_011544503.3:c.4967G= XP_011542805.1:p.Gly1656=
XM_011544504.2:c.4847G= XP_011542806.1:p.Gly1616=
XM_011544505.2:c.4847G= XP_011542807.1:p.Gly1616=
XM_017013319.2:c.5474G= XP_016868808.1:p.Gly1825=
XM_017013320.2:c.5498G= XP_016868809.1:p.Gly1833=
XM_017013321.1:c.5411G= XP_016868810.1:p.Gly1804=
XM_017013322.1:c.5402G= XP_016868811.1:p.Gly1801=
XM_017013323.1:c.5399G= XP_016868812.1:p.Gly1800=
XM_017013324.1:c.5357G= XP_016868813.1:p.Gly1786=
XM_017013325.1:c.5315G= XP_016868814.1:p.Gly1772=
XM_017013326.1:c.5270G= XP_016868815.1:p.Gly1757=
XM_017013327.2:c.5012G= XP_016868816.1:p.Gly1671=
XM_017013328.2:c.4967G= XP_016868817.1:p.Gly1656=
XM_017013329.1:c.4871G= XP_016868818.1:p.Gly1624=
XM_024447128.1:c.5303G= XP_024302896.1:p.Gly1768=
NM_000037.4:c.5234G= MANE Select NP_000028.3:p.Gly1745=
NM_001142446.2:c.5357G= NP_001135918.1:p.Gly1786=
NM_020475.3:c.5234G= NP_065208.2:p.Gly1745=
NM_020476.3:c.5234G= NP_065209.2:p.Gly1745=
NM_020477.3:c.4748G= NP_065210.2:p.Gly1583=