Canonical Allele Identifier: CA1145711442

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041143A= , CM000663.2:g.160041143A=	GRCh38
NC_000001.10:g.160010933A= , CM000663.1:g.160010933A=	GRCh37
NC_000001.9:g.158277557A=	NCBI36
NG_016411.1:g.34029T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+691T=
ENST00000636689.1:n.95-1795T=
ENST00000637644.1:c.487+903T=	ENSP00000490282.1:n.487+903T=
ENST00000638728.1:c.*250T=	ENSP00000492619.1:n.*250T=
ENST00000638840.1:c.919+193T=
ENST00000638868.1:c.*250T=	ENSP00000491250.1:n.*250T=
ENST00000639408.1:c.488-542T=	ENSP00000491635.1:n.488-542T=
ENST00000640017.1:c.670-542T=	ENSP00000491337.1:n.670-542T=
ENST00000640914.1:c.125-542T=
ENST00000644903.1:c.*250T= MANE Select	ENSP00000495557.1:n.*250T=
ENST00000368089.3:c.*250T=	ENSP00000357068.3:n.*250T=
ENST00000509700.1:n.463-542T=
NM_002241.4:c.*250T=	NP_002232.2:n.*250T=
NM_002241.5:c.*250T= MANE Select	NP_002232.2:n.*250T=