Canonical Allele Identifier: CA371051994

Gene: ANK1

Linked Data

• MyVariant Identifiers: chr8:g.41526030C>T (hg19) ; chr8:g.41668512C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41668512C>T , CM000670.2:g.41668512C>T	GRCh38
NC_000008.10:g.41526030C>T , CM000670.1:g.41526030C>T	GRCh37
NC_000008.9:g.41645187C>T	NCBI36
NG_012820.1:g.233251G>A
NG_012820.2:g.233251G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265709.14:c.5272G>A	ENSP00000265709.8:p.Ala1758Thr
ENST00000705521.1:c.5368G>A	ENSP00000516136.1:p.Ala1790Thr
ENST00000705522.1:c.5185G>A	ENSP00000516137.1:p.Ala1729Thr
ENST00000265709.13:c.5272G>A	ENSP00000265709.8:p.Ala1758Thr
ENST00000289734.13:c.5149G>A MANE Select	ENSP00000289734.8:p.Ala1717Thr
ENST00000645531.1:c.1163G>A
ENST00000265709.12:c.5272G>A	ENSP00000265709.8:p.Ala1758Thr
ENST00000289734.11:c.5149G>A	ENSP00000289734.7:p.Ala1717Thr
ENST00000347528.8:c.5149G>A	ENSP00000339620.4:p.Ala1717Thr
ENST00000518061.1:c.721G>A
ENST00000520299.5:c.2627G>A
ENST00000524227.5:n.2543G>A
NM_000037.3:c.5149G>A	NP_000028.3:p.Ala1717Thr
NM_001142446.1:c.5272G>A	NP_001135918.1:p.Ala1758Thr
NM_020475.2:c.5149G>A	NP_065208.2:p.Ala1717Thr
NM_020476.2:c.5149G>A	NP_065209.2:p.Ala1717Thr
NM_020477.2:c.4663G>A	NP_065210.2:p.Ala1555Thr
XM_005273476.3:c.5272G>A	XP_005273533.1:p.Ala1758Thr
XM_011544490.1:c.5413G>A	XP_011542792.1:p.Ala1805Thr
XM_011544491.1:c.5413G>A	XP_011542793.1:p.Ala1805Thr
XM_011544492.1:c.5314G>A	XP_011542794.1:p.Ala1772Thr
XM_011544493.1:c.5413G>A	XP_011542795.1:p.Ala1805Thr
XM_011544494.1:c.5368G>A	XP_011542796.1:p.Ala1790Thr
XM_011544495.1:c.5368G>A	XP_011542797.1:p.Ala1790Thr
XM_011544496.1:c.5413G>A	XP_011542798.1:p.Ala1805Thr
XM_011544497.1:c.5248G>A	XP_011542799.1:p.Ala1750Thr
XM_011544498.1:c.5230G>A	XP_011542800.1:p.Ala1744Thr
XM_011544499.1:c.5413G>A	XP_011542801.1:p.Ala1805Thr
XM_011544500.1:c.5248G>A	XP_011542802.1:p.Ala1750Thr
XM_011544501.1:c.5248G>A	XP_011542803.1:p.Ala1750Thr
XM_011544502.1:c.5248G>A	XP_011542804.1:p.Ala1750Thr
XM_011544503.1:c.4882G>A	XP_011542805.1:p.Ala1628Thr
XM_011544504.1:c.4762G>A	XP_011542806.1:p.Ala1588Thr
XM_011544505.1:c.4762G>A	XP_011542807.1:p.Ala1588Thr
XM_011544506.1:c.4973G>A	XP_011542808.1:p.Cys1658Tyr
XR_949389.1:n.5004G>A
XM_005273476.4:c.5272G>A	XP_005273533.1:p.Ala1758Thr
XM_011544490.3:c.5413G>A	XP_011542792.1:p.Ala1805Thr
XM_011544491.3:c.5413G>A	XP_011542793.1:p.Ala1805Thr
XM_011544494.3:c.5368G>A	XP_011542796.1:p.Ala1790Thr
XM_011544495.3:c.5368G>A	XP_011542797.1:p.Ala1790Thr
XM_011544496.3:c.5413G>A	XP_011542798.1:p.Ala1805Thr
XM_011544500.2:c.5248G>A	XP_011542802.1:p.Ala1750Thr
XM_011544501.2:c.5248G>A	XP_011542803.1:p.Ala1750Thr
XM_011544502.2:c.5248G>A	XP_011542804.1:p.Ala1750Thr
XM_011544503.3:c.4882G>A	XP_011542805.1:p.Ala1628Thr
XM_011544504.2:c.4762G>A	XP_011542806.1:p.Ala1588Thr
XM_011544505.2:c.4762G>A	XP_011542807.1:p.Ala1588Thr
XM_017013319.2:c.5389G>A	XP_016868808.1:p.Ala1797Thr
XM_017013320.2:c.5413G>A	XP_016868809.1:p.Ala1805Thr
XM_017013321.1:c.5326G>A	XP_016868810.1:p.Ala1776Thr
XM_017013322.1:c.5317G>A	XP_016868811.1:p.Ala1773Thr
XM_017013323.1:c.5314G>A	XP_016868812.1:p.Ala1772Thr
XM_017013324.1:c.5272G>A	XP_016868813.1:p.Ala1758Thr
XM_017013325.1:c.5230G>A	XP_016868814.1:p.Ala1744Thr
XM_017013326.1:c.5185G>A	XP_016868815.1:p.Ala1729Thr
XM_017013327.2:c.4927G>A	XP_016868816.1:p.Ala1643Thr
XM_017013328.2:c.4882G>A	XP_016868817.1:p.Ala1628Thr
XM_017013329.1:c.4786G>A	XP_016868818.1:p.Ala1596Thr
XM_024447128.1:c.5218G>A	XP_024302896.1:p.Ala1740Thr
NM_000037.4:c.5149G>A MANE Select	NP_000028.3:p.Ala1717Thr
NM_001142446.2:c.5272G>A	NP_001135918.1:p.Ala1758Thr
NM_020475.3:c.5149G>A	NP_065208.2:p.Ala1717Thr
NM_020476.3:c.5149G>A	NP_065209.2:p.Ala1717Thr
NM_020477.3:c.4663G>A	NP_065210.2:p.Ala1555Thr