Canonical Allele Identifier: CA1141581125

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160042304C= , CM000663.2:g.160042304C=	GRCh38
NC_000001.10:g.160012094C= , CM000663.1:g.160012094C=	GRCh37
NC_000001.9:g.158278718C=	NCBI36
NG_016411.1:g.32868G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.201G=
ENST00000636689.1:n.95-2956G=
ENST00000637644.1:c.229G=	ENSP00000490282.1:p.Gly77=
ENST00000638728.1:c.229G=	ENSP00000492619.1:p.Gly77=
ENST00000638868.1:c.229G=	ENSP00000491250.1:p.Gly77=
ENST00000639408.1:c.229G=	ENSP00000491635.1:p.Gly77=
ENST00000640017.1:c.199G=	ENSP00000491337.1:p.Gly67=
ENST00000644903.1:c.229G= MANE Select	ENSP00000495557.1:p.Gly77=
ENST00000368089.3:c.229G=	ENSP00000357068.3:p.Gly77=
NM_002241.4:c.229G=	NP_002232.2:p.Gly77=
NM_002241.5:c.229G= MANE Select	NP_002232.2:p.Gly77=