Canonical Allele Identifier: CA371051599

Gene: ANK1

Linked Data

• MyVariant Identifiers: chr8:g.41525963G>C (hg19) ; chr8:g.41668445G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41668445G>C , CM000670.2:g.41668445G>C	GRCh38
NC_000008.10:g.41525963G>C , CM000670.1:g.41525963G>C	GRCh37
NC_000008.9:g.41645120G>C	NCBI36
NG_012820.1:g.233318C>G
NG_012820.2:g.233318C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265709.14:c.5339C>G	ENSP00000265709.8:p.Thr1780Ser
ENST00000705521.1:c.5435C>G	ENSP00000516136.1:p.Thr1812Ser
ENST00000705522.1:c.5252C>G	ENSP00000516137.1:p.Thr1751Ser
ENST00000265709.13:c.5339C>G	ENSP00000265709.8:p.Thr1780Ser
ENST00000289734.13:c.5216C>G MANE Select	ENSP00000289734.8:p.Thr1739Ser
ENST00000645531.1:c.1230C>G
ENST00000265709.12:c.5339C>G	ENSP00000265709.8:p.Thr1780Ser
ENST00000289734.11:c.5216C>G	ENSP00000289734.7:p.Thr1739Ser
ENST00000347528.8:c.5216C>G	ENSP00000339620.4:p.Thr1739Ser
ENST00000518061.1:c.788C>G
ENST00000520299.5:c.2694C>G
ENST00000524227.5:n.2610C>G
NM_000037.3:c.5216C>G	NP_000028.3:p.Thr1739Ser
NM_001142446.1:c.5339C>G	NP_001135918.1:p.Thr1780Ser
NM_020475.2:c.5216C>G	NP_065208.2:p.Thr1739Ser
NM_020476.2:c.5216C>G	NP_065209.2:p.Thr1739Ser
NM_020477.2:c.4730C>G	NP_065210.2:p.Thr1577Ser
XM_005273476.3:c.5339C>G	XP_005273533.1:p.Thr1780Ser
XM_011544490.1:c.5480C>G	XP_011542792.1:p.Thr1827Ser
XM_011544491.1:c.5480C>G	XP_011542793.1:p.Thr1827Ser
XM_011544492.1:c.5381C>G	XP_011542794.1:p.Thr1794Ser
XM_011544493.1:c.5480C>G	XP_011542795.1:p.Thr1827Ser
XM_011544494.1:c.5435C>G	XP_011542796.1:p.Thr1812Ser
XM_011544495.1:c.5435C>G	XP_011542797.1:p.Thr1812Ser
XM_011544496.1:c.5480C>G	XP_011542798.1:p.Thr1827Ser
XM_011544497.1:c.5315C>G	XP_011542799.1:p.Thr1772Ser
XM_011544498.1:c.5297C>G	XP_011542800.1:p.Thr1766Ser
XM_011544499.1:c.5480C>G	XP_011542801.1:p.Thr1827Ser
XM_011544500.1:c.5315C>G	XP_011542802.1:p.Thr1772Ser
XM_011544501.1:c.5315C>G	XP_011542803.1:p.Thr1772Ser
XM_011544502.1:c.5315C>G	XP_011542804.1:p.Thr1772Ser
XM_011544503.1:c.4949C>G	XP_011542805.1:p.Thr1650Ser
XM_011544504.1:c.4829C>G	XP_011542806.1:p.Thr1610Ser
XM_011544505.1:c.4829C>G	XP_011542807.1:p.Thr1610Ser
XM_011544506.1:c.5040C>G	XP_011542808.1:p.Asp1680Glu
XR_949389.1:n.5071C>G
XM_005273476.4:c.5339C>G	XP_005273533.1:p.Thr1780Ser
XM_011544490.3:c.5480C>G	XP_011542792.1:p.Thr1827Ser
XM_011544491.3:c.5480C>G	XP_011542793.1:p.Thr1827Ser
XM_011544494.3:c.5435C>G	XP_011542796.1:p.Thr1812Ser
XM_011544495.3:c.5435C>G	XP_011542797.1:p.Thr1812Ser
XM_011544496.3:c.5480C>G	XP_011542798.1:p.Thr1827Ser
XM_011544500.2:c.5315C>G	XP_011542802.1:p.Thr1772Ser
XM_011544501.2:c.5315C>G	XP_011542803.1:p.Thr1772Ser
XM_011544502.2:c.5315C>G	XP_011542804.1:p.Thr1772Ser
XM_011544503.3:c.4949C>G	XP_011542805.1:p.Thr1650Ser
XM_011544504.2:c.4829C>G	XP_011542806.1:p.Thr1610Ser
XM_011544505.2:c.4829C>G	XP_011542807.1:p.Thr1610Ser
XM_017013319.2:c.5456C>G	XP_016868808.1:p.Thr1819Ser
XM_017013320.2:c.5480C>G	XP_016868809.1:p.Thr1827Ser
XM_017013321.1:c.5393C>G	XP_016868810.1:p.Thr1798Ser
XM_017013322.1:c.5384C>G	XP_016868811.1:p.Thr1795Ser
XM_017013323.1:c.5381C>G	XP_016868812.1:p.Thr1794Ser
XM_017013324.1:c.5339C>G	XP_016868813.1:p.Thr1780Ser
XM_017013325.1:c.5297C>G	XP_016868814.1:p.Thr1766Ser
XM_017013326.1:c.5252C>G	XP_016868815.1:p.Thr1751Ser
XM_017013327.2:c.4994C>G	XP_016868816.1:p.Thr1665Ser
XM_017013328.2:c.4949C>G	XP_016868817.1:p.Thr1650Ser
XM_017013329.1:c.4853C>G	XP_016868818.1:p.Thr1618Ser
XM_024447128.1:c.5285C>G	XP_024302896.1:p.Thr1762Ser
NM_000037.4:c.5216C>G MANE Select	NP_000028.3:p.Thr1739Ser
NM_001142446.2:c.5339C>G	NP_001135918.1:p.Thr1780Ser
NM_020475.3:c.5216C>G	NP_065208.2:p.Thr1739Ser
NM_020476.3:c.5216C>G	NP_065209.2:p.Thr1739Ser
NM_020477.3:c.4730C>G	NP_065210.2:p.Thr1577Ser