Canonical Allele Identifier: CA1202156535

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1648588555
• gnomAD v4: 1-160041125-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041125C>A , CM000663.2:g.160041125C>A	GRCh38
NC_000001.10:g.160010915C>A , CM000663.1:g.160010915C>A	GRCh37
NC_000001.9:g.158277539C>A	NCBI36
NG_016411.1:g.34047G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+709G>T
ENST00000636689.1:n.95-1777G>T
ENST00000637644.1:c.487+921G>T	ENSP00000490282.1:n.487+921G>T
ENST00000638728.1:c.*268G>T	ENSP00000492619.1:n.*268G>T
ENST00000638840.1:c.919+211G>T
ENST00000638868.1:c.*268G>T	ENSP00000491250.1:n.*268G>T
ENST00000639408.1:c.488-524G>T	ENSP00000491635.1:n.488-524G>T
ENST00000640017.1:c.670-524G>T	ENSP00000491337.1:n.670-524G>T
ENST00000640914.1:c.125-524G>T
ENST00000644903.1:c.*268G>T MANE Select	ENSP00000495557.1:n.*268G>T
ENST00000368089.3:c.*268G>T	ENSP00000357068.3:n.*268G>T
ENST00000509700.1:n.463-524G>T
NM_002241.4:c.*268G>T	NP_002232.2:n.*268G>T
NM_002241.5:c.*268G>T MANE Select	NP_002232.2:n.*268G>T