Canonical Allele Identifier: CA1141581122

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160042033G= , CM000663.2:g.160042033G=	GRCh38
NC_000001.10:g.160011823G= , CM000663.1:g.160011823G=	GRCh37
NC_000001.9:g.158278447G=	NCBI36
NG_016411.1:g.33139C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.472C=
ENST00000636689.1:n.95-2685C=
ENST00000637644.1:c.487+13C=	ENSP00000490282.1:n.487+13C=
ENST00000638728.1:c.500C=	ENSP00000492619.1:p.Ala167=
ENST00000638840.1:c.222C=
ENST00000638868.1:c.500C=	ENSP00000491250.1:p.Ala167=
ENST00000639408.1:c.487+13C=	ENSP00000491635.1:n.487+13C=
ENST00000640017.1:c.470C=	ENSP00000491337.1:p.Ala157=
ENST00000644903.1:c.500C= MANE Select	ENSP00000495557.1:p.Ala167=
ENST00000368089.3:c.500C=	ENSP00000357068.3:p.Ala167=
ENST00000509700.1:n.263C=
NM_002241.4:c.500C=	NP_002232.2:p.Ala167=
NM_002241.5:c.500C= MANE Select	NP_002232.2:p.Ala167=