Canonical Allele Identifier: CA1202156489

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040995G= , CM000663.2:g.160040995G=	GRCh38
NC_000001.10:g.160010785G= , CM000663.1:g.160010785G=	GRCh37
NC_000001.9:g.158277409G=	NCBI36
NG_016411.1:g.34177C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+839C=
ENST00000636689.1:n.95-1647C=
ENST00000637644.1:c.487+1051C=	ENSP00000490282.1:n.487+1051C=
ENST00000638728.1:c.*398C=	ENSP00000492619.1:n.*398C=
ENST00000638840.1:c.919+341C=
ENST00000638868.1:c.*398C=	ENSP00000491250.1:n.*398C=
ENST00000639408.1:c.488-394C=	ENSP00000491635.1:n.488-394C=
ENST00000640017.1:c.670-394C=	ENSP00000491337.1:n.670-394C=
ENST00000640914.1:c.125-394C=
ENST00000644903.1:c.*398C= MANE Select	ENSP00000495557.1:n.*398C=
ENST00000368089.3:c.*398C=	ENSP00000357068.3:n.*398C=
ENST00000509700.1:n.463-394C=
NM_002241.4:c.*398C=	NP_002232.2:n.*398C=
NM_002241.5:c.*398C= MANE Select	NP_002232.2:n.*398C=