Canonical Allele Identifier: CA1202156497

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041035T= , CM000663.2:g.160041035T=	GRCh38
NC_000001.10:g.160010825T= , CM000663.1:g.160010825T=	GRCh37
NC_000001.9:g.158277449T=	NCBI36
NG_016411.1:g.34137A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+799A=
ENST00000636689.1:n.95-1687A=
ENST00000637644.1:c.487+1011A=	ENSP00000490282.1:n.487+1011A=
ENST00000638728.1:c.*358A=	ENSP00000492619.1:n.*358A=
ENST00000638840.1:c.919+301A=
ENST00000638868.1:c.*358A=	ENSP00000491250.1:n.*358A=
ENST00000639408.1:c.488-434A=	ENSP00000491635.1:n.488-434A=
ENST00000640017.1:c.670-434A=	ENSP00000491337.1:n.670-434A=
ENST00000640914.1:c.125-434A=
ENST00000644903.1:c.*358A= MANE Select	ENSP00000495557.1:n.*358A=
ENST00000368089.3:c.*358A=	ENSP00000357068.3:n.*358A=
ENST00000509700.1:n.463-434A=
NM_002241.4:c.*358A=	NP_002232.2:n.*358A=
NM_002241.5:c.*358A= MANE Select	NP_002232.2:n.*358A=