Canonical Allele Identifier: CA1202156649

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041394C= , CM000663.2:g.160041394C=	GRCh38
NC_000001.10:g.160011184C= , CM000663.1:g.160011184C=	GRCh37
NC_000001.9:g.158277808C=	NCBI36
NG_016411.1:g.33778G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+440G=
ENST00000636689.1:n.95-2046G=
ENST00000637644.1:c.487+652G=	ENSP00000490282.1:n.487+652G=
ENST00000638728.1:c.1139G=	ENSP00000492619.1:p.Ter380=
ENST00000638840.1:c.861G=
ENST00000638868.1:c.1139G=	ENSP00000491250.1:p.Ter380=
ENST00000639408.1:c.487+652G=	ENSP00000491635.1:n.487+652G=
ENST00000640017.1:c.669+440G=	ENSP00000491337.1:n.669+440G=
ENST00000640914.1:c.124+440G=
ENST00000644903.1:c.1139G= MANE Select	ENSP00000495557.1:p.Ter380=
ENST00000368089.3:c.1139G=	ENSP00000357068.3:p.Ter380=
ENST00000509700.1:n.462+440G=
NM_002241.4:c.1139G=	NP_002232.2:p.Ter380=
NM_002241.5:c.1139G= MANE Select	NP_002232.2:p.Ter380=