Canonical Allele Identifier: CA1142728131

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040962G= , CM000663.2:g.160040962G=	GRCh38
NC_000001.10:g.160010752G= , CM000663.1:g.160010752G=	GRCh37
NC_000001.9:g.158277376G=	NCBI36
NG_016411.1:g.34210C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+872C=
ENST00000636689.1:n.95-1614C=
ENST00000637644.1:c.487+1084C=	ENSP00000490282.1:n.487+1084C=
ENST00000638728.1:c.*431C=	ENSP00000492619.1:n.*431C=
ENST00000638840.1:c.920-361C=
ENST00000638868.1:c.*431C=	ENSP00000491250.1:n.*431C=
ENST00000639408.1:c.488-361C=	ENSP00000491635.1:n.488-361C=
ENST00000640017.1:c.670-361C=	ENSP00000491337.1:n.670-361C=
ENST00000640914.1:c.125-361C=
ENST00000644903.1:c.*431C= MANE Select	ENSP00000495557.1:n.*431C=
ENST00000368089.3:c.*431C=	ENSP00000357068.3:n.*431C=
ENST00000509700.1:n.463-361C=
NM_002241.4:c.*431C=	NP_002232.2:n.*431C=
NM_002241.5:c.*431C= MANE Select	NP_002232.2:n.*431C=