Canonical Allele Identifier: CA1141581123

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160042042G= , CM000663.2:g.160042042G=	GRCh38
NC_000001.10:g.160011832G= , CM000663.1:g.160011832G=	GRCh37
NC_000001.9:g.158278456G=	NCBI36
NG_016411.1:g.33130C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.463C=
ENST00000636689.1:n.95-2694C=
ENST00000637644.1:c.487+4C=	ENSP00000490282.1:n.487+4C=
ENST00000638728.1:c.491C=	ENSP00000492619.1:p.Thr164=
ENST00000638840.1:c.213C=
ENST00000638868.1:c.491C=	ENSP00000491250.1:p.Thr164=
ENST00000639408.1:c.487+4C=	ENSP00000491635.1:n.487+4C=
ENST00000640017.1:c.461C=	ENSP00000491337.1:p.Thr154=
ENST00000644903.1:c.491C= MANE Select	ENSP00000495557.1:p.Thr164=
ENST00000368089.3:c.491C=	ENSP00000357068.3:p.Thr164=
ENST00000509700.1:n.254C=
NM_002241.4:c.491C=	NP_002232.2:p.Thr164=
NM_002241.5:c.491C= MANE Select	NP_002232.2:p.Thr164=