Canonical Allele Identifier: CA343223174

Gene: KCNJ10

Linked Data

• MyVariant Identifiers: chr1:g.160011347C>A (hg19) ; chr1:g.160041557C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041557C>A , CM000663.2:g.160041557C>A	GRCh38
NC_000001.10:g.160011347C>A , CM000663.1:g.160011347C>A	GRCh37
NC_000001.9:g.158277971C>A	NCBI36
NG_016411.1:g.33615G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000509700.2:c.671+277G>T
ENST00000636689.1:n.95-2209G>T
ENST00000637644.1:c.487+489G>T	ENSP00000490282.1:n.487+489G>T
ENST00000638728.1:c.976G>T	ENSP00000492619.1:p.Asp326Tyr
ENST00000638840.1:c.698G>T
ENST00000638868.1:c.976G>T	ENSP00000491250.1:p.Asp326Tyr
ENST00000639408.1:c.487+489G>T	ENSP00000491635.1:n.487+489G>T
ENST00000640017.1:c.669+277G>T	ENSP00000491337.1:n.669+277G>T
ENST00000640914.1:c.124+277G>T
ENST00000644903.1:c.976G>T MANE Select	ENSP00000495557.1:p.Asp326Tyr
ENST00000368089.3:c.976G>T	ENSP00000357068.3:p.Asp326Tyr
ENST00000509700.1:n.462+277G>T
NM_002241.4:c.976G>T	NP_002232.2:p.Asp326Tyr
NM_002241.5:c.976G>T MANE Select	NP_002232.2:p.Asp326Tyr