Canonical Allele Identifier: CA1202156702

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041553A= , CM000663.2:g.160041553A=	GRCh38
NC_000001.10:g.160011343A= , CM000663.1:g.160011343A=	GRCh37
NC_000001.9:g.158277967A=	NCBI36
NG_016411.1:g.33619T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+281T=
ENST00000636689.1:n.95-2205T=
ENST00000637644.1:c.487+493T=	ENSP00000490282.1:n.487+493T=
ENST00000638728.1:c.980T=	ENSP00000492619.1:p.Phe327=
ENST00000638840.1:c.702T=
ENST00000638868.1:c.980T=	ENSP00000491250.1:p.Phe327=
ENST00000639408.1:c.487+493T=	ENSP00000491635.1:n.487+493T=
ENST00000640017.1:c.669+281T=	ENSP00000491337.1:n.669+281T=
ENST00000640914.1:c.124+281T=
ENST00000644903.1:c.980T= MANE Select	ENSP00000495557.1:p.Phe327=
ENST00000368089.3:c.980T=	ENSP00000357068.3:p.Phe327=
ENST00000509700.1:n.462+281T=
NM_002241.4:c.980T=	NP_002232.2:p.Phe327=
NM_002241.5:c.980T= MANE Select	NP_002232.2:p.Phe327=