Canonical Allele Identifier: CA1202156485

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1648586109

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040988A>G , CM000663.2:g.160040988A>G	GRCh38
NC_000001.10:g.160010778A>G , CM000663.1:g.160010778A>G	GRCh37
NC_000001.9:g.158277402A>G	NCBI36
NG_016411.1:g.34184T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+846T>C
ENST00000636689.1:n.95-1640T>C
ENST00000637644.1:c.487+1058T>C	ENSP00000490282.1:n.487+1058T>C
ENST00000638728.1:c.*405T>C	ENSP00000492619.1:n.*405T>C
ENST00000638840.1:c.919+348T>C
ENST00000638868.1:c.*405T>C	ENSP00000491250.1:n.*405T>C
ENST00000639408.1:c.488-387T>C	ENSP00000491635.1:n.488-387T>C
ENST00000640017.1:c.670-387T>C	ENSP00000491337.1:n.670-387T>C
ENST00000640914.1:c.125-387T>C
ENST00000644903.1:c.*405T>C MANE Select	ENSP00000495557.1:n.*405T>C
ENST00000368089.3:c.*405T>C	ENSP00000357068.3:n.*405T>C
ENST00000509700.1:n.463-387T>C
NM_002241.4:c.*405T>C	NP_002232.2:n.*405T>C
NM_002241.5:c.*405T>C MANE Select	NP_002232.2:n.*405T>C