Canonical Allele Identifier: CA2574073998

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041387A>T , CM000663.2:g.160041387A>T	GRCh38
NC_000001.10:g.160011177A>T , CM000663.1:g.160011177A>T	GRCh37
NC_000001.9:g.158277801A>T	NCBI36
NG_016411.1:g.33785T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+447T>A
ENST00000636689.1:n.95-2039T>A
ENST00000637644.1:c.487+659T>A	ENSP00000490282.1:n.487+659T>A
ENST00000638728.1:c.*6T>A	ENSP00000492619.1:n.*6T>A
ENST00000638840.1:c.868T>A
ENST00000638868.1:c.*6T>A	ENSP00000491250.1:n.*6T>A
ENST00000639408.1:c.487+659T>A	ENSP00000491635.1:n.487+659T>A
ENST00000640017.1:c.669+447T>A	ENSP00000491337.1:n.669+447T>A
ENST00000640914.1:c.124+447T>A
ENST00000644903.1:c.*6T>A MANE Select	ENSP00000495557.1:n.*6T>A
ENST00000368089.3:c.*6T>A	ENSP00000357068.3:n.*6T>A
ENST00000509700.1:n.462+447T>A
NM_002241.4:c.*6T>A	NP_002232.2:n.*6T>A
NM_002241.5:c.*6T>A MANE Select	NP_002232.2:n.*6T>A