Canonical Allele Identifier: CA2648631722

Gene: KCNJ10

Linked Data

• gnomAD v4: 1-160041331-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041333del , CM000663.2:g.160041333del	GRCh38
NC_000001.10:g.160011123del , CM000663.1:g.160011123del	GRCh37
NC_000001.9:g.158277747del	NCBI36
NG_016411.1:g.33840del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+502del
ENST00000636689.1:n.95-1984del
ENST00000637644.1:c.487+714del	ENSP00000490282.1:n.487+714del
ENST00000638728.1:c.*61del	ENSP00000492619.1:n.*61del
ENST00000638840.1:c.919+4del
ENST00000638868.1:c.*61del	ENSP00000491250.1:n.*61del
ENST00000639408.1:c.487+714del	ENSP00000491635.1:n.487+714del
ENST00000640017.1:c.669+502del	ENSP00000491337.1:n.669+502del
ENST00000640914.1:c.124+502del
ENST00000644903.1:c.*61del MANE Select	ENSP00000495557.1:n.*61del
ENST00000368089.3:c.*61del	ENSP00000357068.3:n.*61del
ENST00000509700.1:n.462+502del
NM_002241.4:c.*61del	NP_002232.2:n.*61del
NM_002241.5:c.*61del MANE Select	NP_002232.2:n.*61del