Canonical Allele Identifier: CA2648631430

Gene: KCNJ10

Linked Data

• gnomAD v4: 1-160041010-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041012del , CM000663.2:g.160041012del	GRCh38
NC_000001.10:g.160010802del , CM000663.1:g.160010802del	GRCh37
NC_000001.9:g.158277426del	NCBI36
NG_016411.1:g.34161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+823del
ENST00000636689.1:n.95-1663del
ENST00000637644.1:c.487+1035del	ENSP00000490282.1:n.487+1035del
ENST00000638728.1:c.*382del	ENSP00000492619.1:n.*382del
ENST00000638840.1:c.919+325del
ENST00000638868.1:c.*382del	ENSP00000491250.1:n.*382del
ENST00000639408.1:c.488-410del	ENSP00000491635.1:n.488-410del
ENST00000640017.1:c.670-410del	ENSP00000491337.1:n.670-410del
ENST00000640914.1:c.125-410del
ENST00000644903.1:c.*382del MANE Select	ENSP00000495557.1:n.*382del
ENST00000368089.3:c.*382del	ENSP00000357068.3:n.*382del
ENST00000509700.1:n.463-410del
NM_002241.4:c.*382del	NP_002232.2:n.*382del
NM_002241.5:c.*382del MANE Select	NP_002232.2:n.*382del