Canonical Allele Identifier: CA371051411

Gene: ANK1

Linked Data

• MyVariant Identifiers: chr8:g.41525919G>T (hg19) ; chr8:g.41668401G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41668401G>T , CM000670.2:g.41668401G>T	GRCh38
NC_000008.10:g.41525919G>T , CM000670.1:g.41525919G>T	GRCh37
NC_000008.9:g.41645076G>T	NCBI36
NG_012820.1:g.233362C>A
NG_012820.2:g.233362C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265709.14:c.5383C>A	ENSP00000265709.8:p.Leu1795Met
ENST00000705521.1:c.5479C>A	ENSP00000516136.1:p.Leu1827Met
ENST00000705522.1:c.5296C>A	ENSP00000516137.1:p.Leu1766Met
ENST00000265709.13:c.5383C>A	ENSP00000265709.8:p.Leu1795Met
ENST00000289734.13:c.5260C>A MANE Select	ENSP00000289734.8:p.Leu1754Met
ENST00000645531.1:c.1274C>A
ENST00000265709.12:c.5383C>A	ENSP00000265709.8:p.Leu1795Met
ENST00000289734.11:c.5260C>A	ENSP00000289734.7:p.Leu1754Met
ENST00000347528.8:c.5260C>A	ENSP00000339620.4:p.Leu1754Met
ENST00000518061.1:c.832C>A
ENST00000520299.5:c.2738C>A
ENST00000524227.5:n.2654C>A
NM_000037.3:c.5260C>A	NP_000028.3:p.Leu1754Met
NM_001142446.1:c.5383C>A	NP_001135918.1:p.Leu1795Met
NM_020475.2:c.5260C>A	NP_065208.2:p.Leu1754Met
NM_020476.2:c.5260C>A	NP_065209.2:p.Leu1754Met
NM_020477.2:c.4774C>A	NP_065210.2:p.Leu1592Met
XM_005273476.3:c.5383C>A	XP_005273533.1:p.Leu1795Met
XM_011544490.1:c.5524C>A	XP_011542792.1:p.Leu1842Met
XM_011544491.1:c.5524C>A	XP_011542793.1:p.Leu1842Met
XM_011544492.1:c.5425C>A	XP_011542794.1:p.Leu1809Met
XM_011544493.1:c.5524C>A	XP_011542795.1:p.Leu1842Met
XM_011544494.1:c.5479C>A	XP_011542796.1:p.Leu1827Met
XM_011544495.1:c.5479C>A	XP_011542797.1:p.Leu1827Met
XM_011544496.1:c.5524C>A	XP_011542798.1:p.Leu1842Met
XM_011544497.1:c.5359C>A	XP_011542799.1:p.Leu1787Met
XM_011544498.1:c.5341C>A	XP_011542800.1:p.Leu1781Met
XM_011544499.1:c.5524C>A	XP_011542801.1:p.Leu1842Met
XM_011544500.1:c.5359C>A	XP_011542802.1:p.Leu1787Met
XM_011544501.1:c.5359C>A	XP_011542803.1:p.Leu1787Met
XM_011544502.1:c.5359C>A	XP_011542804.1:p.Leu1787Met
XM_011544503.1:c.4993C>A	XP_011542805.1:p.Leu1665Met
XM_011544504.1:c.4873C>A	XP_011542806.1:p.Leu1625Met
XM_011544505.1:c.4873C>A	XP_011542807.1:p.Leu1625Met
XM_011544506.1:c.*41C>A	XP_011542808.1:n.*41C>A
XR_949389.1:n.5115C>A
XM_005273476.4:c.5383C>A	XP_005273533.1:p.Leu1795Met
XM_011544490.3:c.5524C>A	XP_011542792.1:p.Leu1842Met
XM_011544491.3:c.5524C>A	XP_011542793.1:p.Leu1842Met
XM_011544494.3:c.5479C>A	XP_011542796.1:p.Leu1827Met
XM_011544495.3:c.5479C>A	XP_011542797.1:p.Leu1827Met
XM_011544496.3:c.5524C>A	XP_011542798.1:p.Leu1842Met
XM_011544500.2:c.5359C>A	XP_011542802.1:p.Leu1787Met
XM_011544501.2:c.5359C>A	XP_011542803.1:p.Leu1787Met
XM_011544502.2:c.5359C>A	XP_011542804.1:p.Leu1787Met
XM_011544503.3:c.4993C>A	XP_011542805.1:p.Leu1665Met
XM_011544504.2:c.4873C>A	XP_011542806.1:p.Leu1625Met
XM_011544505.2:c.4873C>A	XP_011542807.1:p.Leu1625Met
XM_017013319.2:c.5500C>A	XP_016868808.1:p.Leu1834Met
XM_017013320.2:c.5524C>A	XP_016868809.1:p.Leu1842Met
XM_017013321.1:c.5437C>A	XP_016868810.1:p.Leu1813Met
XM_017013322.1:c.5428C>A	XP_016868811.1:p.Leu1810Met
XM_017013323.1:c.5425C>A	XP_016868812.1:p.Leu1809Met
XM_017013324.1:c.5383C>A	XP_016868813.1:p.Leu1795Met
XM_017013325.1:c.5341C>A	XP_016868814.1:p.Leu1781Met
XM_017013326.1:c.5296C>A	XP_016868815.1:p.Leu1766Met
XM_017013327.2:c.5038C>A	XP_016868816.1:p.Leu1680Met
XM_017013328.2:c.4993C>A	XP_016868817.1:p.Leu1665Met
XM_017013329.1:c.4897C>A	XP_016868818.1:p.Leu1633Met
XM_024447128.1:c.5329C>A	XP_024302896.1:p.Leu1777Met
NM_000037.4:c.5260C>A MANE Select	NP_000028.3:p.Leu1754Met
NM_001142446.2:c.5383C>A	NP_001135918.1:p.Leu1795Met
NM_020475.3:c.5260C>A	NP_065208.2:p.Leu1754Met
NM_020476.3:c.5260C>A	NP_065209.2:p.Leu1754Met
NM_020477.3:c.4774C>A	NP_065210.2:p.Leu1592Met