Canonical Allele Identifier: CA2648631684

Gene: KCNJ10

Linked Data

• gnomAD v4: 1-160041290-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041293del , CM000663.2:g.160041293del	GRCh38
NC_000001.10:g.160011083del , CM000663.1:g.160011083del	GRCh37
NC_000001.9:g.158277707del	NCBI36
NG_016411.1:g.33881del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+543del
ENST00000636689.1:n.95-1943del
ENST00000637644.1:c.487+755del	ENSP00000490282.1:n.487+755del
ENST00000638728.1:c.*102del	ENSP00000492619.1:n.*102del
ENST00000638840.1:c.919+45del
ENST00000638868.1:c.*102del	ENSP00000491250.1:n.*102del
ENST00000639408.1:c.488-690del	ENSP00000491635.1:n.488-690del
ENST00000640017.1:c.669+543del	ENSP00000491337.1:n.669+543del
ENST00000640914.1:c.124+543del
ENST00000644903.1:c.*102del MANE Select	ENSP00000495557.1:n.*102del
ENST00000368089.3:c.*102del	ENSP00000357068.3:n.*102del
ENST00000509700.1:n.462+543del
NM_002241.4:c.*102del	NP_002232.2:n.*102del
NM_002241.5:c.*102del MANE Select	NP_002232.2:n.*102del