Canonical Allele Identifier: CA371052252

Gene: ANK1

Linked Data

• MyVariant Identifiers: chr8:g.41526070C>T (hg19) ; chr8:g.41668552C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41668552C>T , CM000670.2:g.41668552C>T	GRCh38
NC_000008.10:g.41526070C>T , CM000670.1:g.41526070C>T	GRCh37
NC_000008.9:g.41645227C>T	NCBI36
NG_012820.1:g.233211G>A
NG_012820.2:g.233211G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265709.14:c.5232G>A	ENSP00000265709.8:p.Trp1744Ter
ENST00000705521.1:c.5328G>A	ENSP00000516136.1:p.Trp1776Ter
ENST00000705522.1:c.5145G>A	ENSP00000516137.1:p.Trp1715Ter
ENST00000265709.13:c.5232G>A	ENSP00000265709.8:p.Trp1744Ter
ENST00000289734.13:c.5109G>A MANE Select	ENSP00000289734.8:p.Trp1703Ter
ENST00000645531.1:c.1123G>A
ENST00000265709.12:c.5232G>A	ENSP00000265709.8:p.Trp1744Ter
ENST00000289734.11:c.5109G>A	ENSP00000289734.7:p.Trp1703Ter
ENST00000347528.8:c.5109G>A	ENSP00000339620.4:p.Trp1703Ter
ENST00000518061.1:c.681G>A
ENST00000520299.5:c.2587G>A
ENST00000524227.5:n.2503G>A
NM_000037.3:c.5109G>A	NP_000028.3:p.Trp1703Ter
NM_001142446.1:c.5232G>A	NP_001135918.1:p.Trp1744Ter
NM_020475.2:c.5109G>A	NP_065208.2:p.Trp1703Ter
NM_020476.2:c.5109G>A	NP_065209.2:p.Trp1703Ter
NM_020477.2:c.4623G>A	NP_065210.2:p.Trp1541Ter
XM_005273476.3:c.5232G>A	XP_005273533.1:p.Trp1744Ter
XM_011544490.1:c.5373G>A	XP_011542792.1:p.Trp1791Ter
XM_011544491.1:c.5373G>A	XP_011542793.1:p.Trp1791Ter
XM_011544492.1:c.5274G>A	XP_011542794.1:p.Trp1758Ter
XM_011544493.1:c.5373G>A	XP_011542795.1:p.Trp1791Ter
XM_011544494.1:c.5328G>A	XP_011542796.1:p.Trp1776Ter
XM_011544495.1:c.5328G>A	XP_011542797.1:p.Trp1776Ter
XM_011544496.1:c.5373G>A	XP_011542798.1:p.Trp1791Ter
XM_011544497.1:c.5208G>A	XP_011542799.1:p.Trp1736Ter
XM_011544498.1:c.5190G>A	XP_011542800.1:p.Trp1730Ter
XM_011544499.1:c.5373G>A	XP_011542801.1:p.Trp1791Ter
XM_011544500.1:c.5208G>A	XP_011542802.1:p.Trp1736Ter
XM_011544501.1:c.5208G>A	XP_011542803.1:p.Trp1736Ter
XM_011544502.1:c.5208G>A	XP_011542804.1:p.Trp1736Ter
XM_011544503.1:c.4842G>A	XP_011542805.1:p.Trp1614Ter
XM_011544504.1:c.4722G>A	XP_011542806.1:p.Trp1574Ter
XM_011544505.1:c.4722G>A	XP_011542807.1:p.Trp1574Ter
XM_011544506.1:c.4933G>A	XP_011542808.1:p.Gly1645Arg
XR_949389.1:n.4964G>A
XM_005273476.4:c.5232G>A	XP_005273533.1:p.Trp1744Ter
XM_011544490.3:c.5373G>A	XP_011542792.1:p.Trp1791Ter
XM_011544491.3:c.5373G>A	XP_011542793.1:p.Trp1791Ter
XM_011544494.3:c.5328G>A	XP_011542796.1:p.Trp1776Ter
XM_011544495.3:c.5328G>A	XP_011542797.1:p.Trp1776Ter
XM_011544496.3:c.5373G>A	XP_011542798.1:p.Trp1791Ter
XM_011544500.2:c.5208G>A	XP_011542802.1:p.Trp1736Ter
XM_011544501.2:c.5208G>A	XP_011542803.1:p.Trp1736Ter
XM_011544502.2:c.5208G>A	XP_011542804.1:p.Trp1736Ter
XM_011544503.3:c.4842G>A	XP_011542805.1:p.Trp1614Ter
XM_011544504.2:c.4722G>A	XP_011542806.1:p.Trp1574Ter
XM_011544505.2:c.4722G>A	XP_011542807.1:p.Trp1574Ter
XM_017013319.2:c.5349G>A	XP_016868808.1:p.Trp1783Ter
XM_017013320.2:c.5373G>A	XP_016868809.1:p.Trp1791Ter
XM_017013321.1:c.5286G>A	XP_016868810.1:p.Trp1762Ter
XM_017013322.1:c.5277G>A	XP_016868811.1:p.Trp1759Ter
XM_017013323.1:c.5274G>A	XP_016868812.1:p.Trp1758Ter
XM_017013324.1:c.5232G>A	XP_016868813.1:p.Trp1744Ter
XM_017013325.1:c.5190G>A	XP_016868814.1:p.Trp1730Ter
XM_017013326.1:c.5145G>A	XP_016868815.1:p.Trp1715Ter
XM_017013327.2:c.4887G>A	XP_016868816.1:p.Trp1629Ter
XM_017013328.2:c.4842G>A	XP_016868817.1:p.Trp1614Ter
XM_017013329.1:c.4746G>A	XP_016868818.1:p.Trp1582Ter
XM_024447128.1:c.5178G>A	XP_024302896.1:p.Trp1726Ter
NM_000037.4:c.5109G>A MANE Select	NP_000028.3:p.Trp1703Ter
NM_001142446.2:c.5232G>A	NP_001135918.1:p.Trp1744Ter
NM_020475.3:c.5109G>A	NP_065208.2:p.Trp1703Ter
NM_020476.3:c.5109G>A	NP_065209.2:p.Trp1703Ter
NM_020477.3:c.4623G>A	NP_065210.2:p.Trp1541Ter