Canonical Allele Identifier: CA1202156682

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041505C= , CM000663.2:g.160041505C=	GRCh38
NC_000001.10:g.160011295C= , CM000663.1:g.160011295C=	GRCh37
NC_000001.9:g.158277919C=	NCBI36
NG_016411.1:g.33667G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000509700.2:c.671+329G=
ENST00000636689.1:n.95-2157G=
ENST00000637644.1:c.487+541G=	ENSP00000490282.1:n.487+541G=
ENST00000638728.1:c.1028G=	ENSP00000492619.1:p.Arg343=
ENST00000638840.1:c.750G=
ENST00000638868.1:c.1028G=	ENSP00000491250.1:p.Arg343=
ENST00000639408.1:c.487+541G=	ENSP00000491635.1:n.487+541G=
ENST00000640017.1:c.669+329G=	ENSP00000491337.1:n.669+329G=
ENST00000640914.1:c.124+329G=
ENST00000644903.1:c.1028G= MANE Select	ENSP00000495557.1:p.Arg343=
ENST00000368089.3:c.1028G=	ENSP00000357068.3:p.Arg343=
ENST00000509700.1:n.462+329G=
NM_002241.4:c.1028G=	NP_002232.2:p.Arg343=
NM_002241.5:c.1028G= MANE Select	NP_002232.2:p.Arg343=