Canonical Allele Identifier: CA1144229025

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160042340G= , CM000663.2:g.160042340G=	GRCh38
NC_000001.10:g.160012130G= , CM000663.1:g.160012130G=	GRCh37
NC_000001.9:g.158278754G=	NCBI36
NG_016411.1:g.32832C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.165C=
ENST00000636689.1:n.95-2992C=
ENST00000637644.1:c.193C=	ENSP00000490282.1:p.Arg65=
ENST00000638728.1:c.193C=	ENSP00000492619.1:p.Arg65=
ENST00000638868.1:c.193C=	ENSP00000491250.1:p.Arg65=
ENST00000639408.1:c.193C=	ENSP00000491635.1:p.Arg65=
ENST00000640017.1:c.163C=	ENSP00000491337.1:p.Arg55=
ENST00000644903.1:c.193C= MANE Select	ENSP00000495557.1:p.Arg65=
ENST00000368089.3:c.193C=	ENSP00000357068.3:p.Arg65=
NM_002241.4:c.193C=	NP_002232.2:p.Arg65=
NM_002241.5:c.193C= MANE Select	NP_002232.2:p.Arg65=