Canonical Allele Identifier: CA1202156698

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041549G= , CM000663.2:g.160041549G=	GRCh38
NC_000001.10:g.160011339G= , CM000663.1:g.160011339G=	GRCh37
NC_000001.9:g.158277963G=	NCBI36
NG_016411.1:g.33623C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+285C=
ENST00000636689.1:n.95-2201C=
ENST00000637644.1:c.487+497C=	ENSP00000490282.1:n.487+497C=
ENST00000638728.1:c.984C=	ENSP00000492619.1:p.Ser328=
ENST00000638840.1:c.706C=
ENST00000638868.1:c.984C=	ENSP00000491250.1:p.Ser328=
ENST00000639408.1:c.487+497C=	ENSP00000491635.1:n.487+497C=
ENST00000640017.1:c.669+285C=	ENSP00000491337.1:n.669+285C=
ENST00000640914.1:c.124+285C=
ENST00000644903.1:c.984C= MANE Select	ENSP00000495557.1:p.Ser328=
ENST00000368089.3:c.984C=	ENSP00000357068.3:p.Ser328=
ENST00000509700.1:n.462+285C=
NM_002241.4:c.984C=	NP_002232.2:p.Ser328=
NM_002241.5:c.984C= MANE Select	NP_002232.2:p.Ser328=