Canonical Allele Identifier: CA343230618

Gene: KCNJ10

Linked Data

• COSMIC: COSM6121859 ; COSM6121860
• MyVariant Identifiers: chr1:g.160012258C>G (hg19) ; chr1:g.160042468C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160042468C>G , CM000663.2:g.160042468C>G	GRCh38
NC_000001.10:g.160012258C>G , CM000663.1:g.160012258C>G	GRCh37
NC_000001.9:g.158278882C>G	NCBI36
NG_016411.1:g.32704G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.37G>C
ENST00000636689.1:n.95-3120G>C
ENST00000637644.1:c.65G>C	ENSP00000490282.1:p.Gly22Ala
ENST00000638728.1:c.65G>C	ENSP00000492619.1:p.Gly22Ala
ENST00000638868.1:c.65G>C	ENSP00000491250.1:p.Gly22Ala
ENST00000639408.1:c.65G>C	ENSP00000491635.1:p.Gly22Ala
ENST00000640017.1:c.35G>C	ENSP00000491337.1:p.Gly12Ala
ENST00000644903.1:c.65G>C MANE Select	ENSP00000495557.1:p.Gly22Ala
ENST00000368089.3:c.65G>C	ENSP00000357068.3:p.Gly22Ala
NM_002241.4:c.65G>C	NP_002232.2:p.Gly22Ala
NM_002241.5:c.65G>C MANE Select	NP_002232.2:p.Gly22Ala