Canonical Allele Identifier: CA460782097

Gene: ANK1

Linked Data

• MyVariant Identifiers: chr8:g.41526013T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41668495T>C , CM000670.2:g.41668495T>C	GRCh38
NC_000008.10:g.41526013T>C , CM000670.1:g.41526013T>C	GRCh37
NC_000008.9:g.41645170T>C	NCBI36
NG_012820.1:g.233268A>G
NG_012820.2:g.233268A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265709.14:c.5289A>G	ENSP00000265709.8:p.Gln1763=
ENST00000705521.1:c.5385A>G	ENSP00000516136.1:p.Gln1795=
ENST00000705522.1:c.5202A>G	ENSP00000516137.1:p.Gln1734=
ENST00000265709.13:c.5289A>G	ENSP00000265709.8:p.Gln1763=
ENST00000289734.13:c.5166A>G MANE Select	ENSP00000289734.8:p.Gln1722=
ENST00000645531.1:c.1180A>G
ENST00000265709.12:c.5289A>G	ENSP00000265709.8:p.Gln1763=
ENST00000289734.11:c.5166A>G	ENSP00000289734.7:p.Gln1722=
ENST00000347528.8:c.5166A>G	ENSP00000339620.4:p.Gln1722=
ENST00000518061.1:c.738A>G
ENST00000520299.5:c.2644A>G
ENST00000524227.5:n.2560A>G
NM_000037.3:c.5166A>G	NP_000028.3:p.Gln1722=
NM_001142446.1:c.5289A>G	NP_001135918.1:p.Gln1763=
NM_020475.2:c.5166A>G	NP_065208.2:p.Gln1722=
NM_020476.2:c.5166A>G	NP_065209.2:p.Gln1722=
NM_020477.2:c.4680A>G	NP_065210.2:p.Gln1560=
XM_005273476.3:c.5289A>G	XP_005273533.1:p.Gln1763=
XM_011544490.1:c.5430A>G	XP_011542792.1:p.Gln1810=
XM_011544491.1:c.5430A>G	XP_011542793.1:p.Gln1810=
XM_011544492.1:c.5331A>G	XP_011542794.1:p.Gln1777=
XM_011544493.1:c.5430A>G	XP_011542795.1:p.Gln1810=
XM_011544494.1:c.5385A>G	XP_011542796.1:p.Gln1795=
XM_011544495.1:c.5385A>G	XP_011542797.1:p.Gln1795=
XM_011544496.1:c.5430A>G	XP_011542798.1:p.Gln1810=
XM_011544497.1:c.5265A>G	XP_011542799.1:p.Gln1755=
XM_011544498.1:c.5247A>G	XP_011542800.1:p.Gln1749=
XM_011544499.1:c.5430A>G	XP_011542801.1:p.Gln1810=
XM_011544500.1:c.5265A>G	XP_011542802.1:p.Gln1755=
XM_011544501.1:c.5265A>G	XP_011542803.1:p.Gln1755=
XM_011544502.1:c.5265A>G	XP_011542804.1:p.Gln1755=
XM_011544503.1:c.4899A>G	XP_011542805.1:p.Gln1633=
XM_011544504.1:c.4779A>G	XP_011542806.1:p.Gln1593=
XM_011544505.1:c.4779A>G	XP_011542807.1:p.Gln1593=
XM_011544506.1:c.4990A>G	XP_011542808.1:p.Arg1664Gly
XR_949389.1:n.5021A>G
XM_005273476.4:c.5289A>G	XP_005273533.1:p.Gln1763=
XM_011544490.3:c.5430A>G	XP_011542792.1:p.Gln1810=
XM_011544491.3:c.5430A>G	XP_011542793.1:p.Gln1810=
XM_011544494.3:c.5385A>G	XP_011542796.1:p.Gln1795=
XM_011544495.3:c.5385A>G	XP_011542797.1:p.Gln1795=
XM_011544496.3:c.5430A>G	XP_011542798.1:p.Gln1810=
XM_011544500.2:c.5265A>G	XP_011542802.1:p.Gln1755=
XM_011544501.2:c.5265A>G	XP_011542803.1:p.Gln1755=
XM_011544502.2:c.5265A>G	XP_011542804.1:p.Gln1755=
XM_011544503.3:c.4899A>G	XP_011542805.1:p.Gln1633=
XM_011544504.2:c.4779A>G	XP_011542806.1:p.Gln1593=
XM_011544505.2:c.4779A>G	XP_011542807.1:p.Gln1593=
XM_017013319.2:c.5406A>G	XP_016868808.1:p.Gln1802=
XM_017013320.2:c.5430A>G	XP_016868809.1:p.Gln1810=
XM_017013321.1:c.5343A>G	XP_016868810.1:p.Gln1781=
XM_017013322.1:c.5334A>G	XP_016868811.1:p.Gln1778=
XM_017013323.1:c.5331A>G	XP_016868812.1:p.Gln1777=
XM_017013324.1:c.5289A>G	XP_016868813.1:p.Gln1763=
XM_017013325.1:c.5247A>G	XP_016868814.1:p.Gln1749=
XM_017013326.1:c.5202A>G	XP_016868815.1:p.Gln1734=
XM_017013327.2:c.4944A>G	XP_016868816.1:p.Gln1648=
XM_017013328.2:c.4899A>G	XP_016868817.1:p.Gln1633=
XM_017013329.1:c.4803A>G	XP_016868818.1:p.Gln1601=
XM_024447128.1:c.5235A>G	XP_024302896.1:p.Gln1745=
NM_000037.4:c.5166A>G MANE Select	NP_000028.3:p.Gln1722=
NM_001142446.2:c.5289A>G	NP_001135918.1:p.Gln1763=
NM_020475.3:c.5166A>G	NP_065208.2:p.Gln1722=
NM_020476.3:c.5166A>G	NP_065209.2:p.Gln1722=
NM_020477.3:c.4680A>G	NP_065210.2:p.Gln1560=