Canonical Allele Identifier: CA371051406

Gene: ANK1

Linked Data

• gnomAD v4: 8-41668398-C-T
• MyVariant Identifiers: chr8:g.41525916C>T (hg19) ; chr8:g.41668398C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41668398C>T , CM000670.2:g.41668398C>T	GRCh38
NC_000008.10:g.41525916C>T , CM000670.1:g.41525916C>T	GRCh37
NC_000008.9:g.41645073C>T	NCBI36
NG_012820.1:g.233365G>A
NG_012820.2:g.233365G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265709.14:c.5386G>A	ENSP00000265709.8:p.Val1796Met
ENST00000705521.1:c.5482G>A	ENSP00000516136.1:p.Val1828Met
ENST00000705522.1:c.5299G>A	ENSP00000516137.1:p.Val1767Met
ENST00000265709.13:c.5386G>A	ENSP00000265709.8:p.Val1796Met
ENST00000289734.13:c.5263G>A MANE Select	ENSP00000289734.8:p.Val1755Met
ENST00000645531.1:c.1277G>A
ENST00000265709.12:c.5386G>A	ENSP00000265709.8:p.Val1796Met
ENST00000289734.11:c.5263G>A	ENSP00000289734.7:p.Val1755Met
ENST00000347528.8:c.5263G>A	ENSP00000339620.4:p.Val1755Met
ENST00000518061.1:c.835G>A
ENST00000520299.5:c.2741G>A
ENST00000524227.5:n.2657G>A
NM_000037.3:c.5263G>A	NP_000028.3:p.Val1755Met
NM_001142446.1:c.5386G>A	NP_001135918.1:p.Val1796Met
NM_020475.2:c.5263G>A	NP_065208.2:p.Val1755Met
NM_020476.2:c.5263G>A	NP_065209.2:p.Val1755Met
NM_020477.2:c.4777G>A	NP_065210.2:p.Val1593Met
XM_005273476.3:c.5386G>A	XP_005273533.1:p.Val1796Met
XM_011544490.1:c.5527G>A	XP_011542792.1:p.Val1843Met
XM_011544491.1:c.5527G>A	XP_011542793.1:p.Val1843Met
XM_011544492.1:c.5428G>A	XP_011542794.1:p.Val1810Met
XM_011544493.1:c.5527G>A	XP_011542795.1:p.Val1843Met
XM_011544494.1:c.5482G>A	XP_011542796.1:p.Val1828Met
XM_011544495.1:c.5482G>A	XP_011542797.1:p.Val1828Met
XM_011544496.1:c.5527G>A	XP_011542798.1:p.Val1843Met
XM_011544497.1:c.5362G>A	XP_011542799.1:p.Val1788Met
XM_011544498.1:c.5344G>A	XP_011542800.1:p.Val1782Met
XM_011544499.1:c.5527G>A	XP_011542801.1:p.Val1843Met
XM_011544500.1:c.5362G>A	XP_011542802.1:p.Val1788Met
XM_011544501.1:c.5362G>A	XP_011542803.1:p.Val1788Met
XM_011544502.1:c.5362G>A	XP_011542804.1:p.Val1788Met
XM_011544503.1:c.4996G>A	XP_011542805.1:p.Val1666Met
XM_011544504.1:c.4876G>A	XP_011542806.1:p.Val1626Met
XM_011544505.1:c.4876G>A	XP_011542807.1:p.Val1626Met
XM_011544506.1:c.*44G>A	XP_011542808.1:n.*44G>A
XR_949389.1:n.5118G>A
XM_005273476.4:c.5386G>A	XP_005273533.1:p.Val1796Met
XM_011544490.3:c.5527G>A	XP_011542792.1:p.Val1843Met
XM_011544491.3:c.5527G>A	XP_011542793.1:p.Val1843Met
XM_011544494.3:c.5482G>A	XP_011542796.1:p.Val1828Met
XM_011544495.3:c.5482G>A	XP_011542797.1:p.Val1828Met
XM_011544496.3:c.5527G>A	XP_011542798.1:p.Val1843Met
XM_011544500.2:c.5362G>A	XP_011542802.1:p.Val1788Met
XM_011544501.2:c.5362G>A	XP_011542803.1:p.Val1788Met
XM_011544502.2:c.5362G>A	XP_011542804.1:p.Val1788Met
XM_011544503.3:c.4996G>A	XP_011542805.1:p.Val1666Met
XM_011544504.2:c.4876G>A	XP_011542806.1:p.Val1626Met
XM_011544505.2:c.4876G>A	XP_011542807.1:p.Val1626Met
XM_017013319.2:c.5503G>A	XP_016868808.1:p.Val1835Met
XM_017013320.2:c.5527G>A	XP_016868809.1:p.Val1843Met
XM_017013321.1:c.5440G>A	XP_016868810.1:p.Val1814Met
XM_017013322.1:c.5431G>A	XP_016868811.1:p.Val1811Met
XM_017013323.1:c.5428G>A	XP_016868812.1:p.Val1810Met
XM_017013324.1:c.5386G>A	XP_016868813.1:p.Val1796Met
XM_017013325.1:c.5344G>A	XP_016868814.1:p.Val1782Met
XM_017013326.1:c.5299G>A	XP_016868815.1:p.Val1767Met
XM_017013327.2:c.5041G>A	XP_016868816.1:p.Val1681Met
XM_017013328.2:c.4996G>A	XP_016868817.1:p.Val1666Met
XM_017013329.1:c.4900G>A	XP_016868818.1:p.Val1634Met
XM_024447128.1:c.5332G>A	XP_024302896.1:p.Val1778Met
NM_000037.4:c.5263G>A MANE Select	NP_000028.3:p.Val1755Met
NM_001142446.2:c.5386G>A	NP_001135918.1:p.Val1796Met
NM_020475.3:c.5263G>A	NP_065208.2:p.Val1755Met
NM_020476.3:c.5263G>A	NP_065209.2:p.Val1755Met
NM_020477.3:c.4777G>A	NP_065210.2:p.Val1593Met