Canonical Allele Identifier: CA31469608

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041127A>T , CM000663.2:g.160041127A>T	GRCh38
NC_000001.10:g.160010917A>T , CM000663.1:g.160010917A>T	GRCh37
NC_000001.9:g.158277541A>T	NCBI36
NG_016411.1:g.34045T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002241.5:c.*266T>A MANE Select	NP_002232.2:n.*266T>A
ENST00000644903.1:c.*266T>A MANE Select	ENSP00000495557.1:n.*266T>A
NM_002241.4:c.*266T>A	NP_002232.2:n.*266T>A
ENST00000368089.3:c.*266T>A	ENSP00000357068.3:n.*266T>A
ENST00000509700.1:n.463-526T>A
ENST00000509700.2:c.671+707T>A
ENST00000636689.1:n.95-1779T>A
ENST00000637644.1:c.487+919T>A	ENSP00000490282.1:n.487+919T>A
ENST00000638728.1:c.*266T>A	ENSP00000492619.1:n.*266T>A
ENST00000638840.1:c.919+209T>A
ENST00000638868.1:c.*266T>A	ENSP00000491250.1:n.*266T>A
ENST00000639408.1:c.488-526T>A	ENSP00000491635.1:n.488-526T>A
ENST00000640017.1:c.670-526T>A	ENSP00000491337.1:n.670-526T>A
ENST00000640914.1:c.125-526T>A