Canonical Allele Identifier: CA2648631453

Gene: KCNJ10

Linked Data

• gnomAD v4: 1-160041034-ATGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041044_160041046del , CM000663.2:g.160041044_160041046del	GRCh38
NC_000001.10:g.160010834_160010836del , CM000663.1:g.160010834_160010836del	GRCh37
NC_000001.9:g.158277458_158277460del	NCBI36
NG_016411.1:g.34135_34137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+797_671+799del
ENST00000636689.1:n.95-1689_95-1687del
ENST00000637644.1:c.487+1009_487+1011del	ENSP00000490282.1:n.487+1009_487+1011del
ENST00000638728.1:c.*356_*358del	ENSP00000492619.1:n.*356_*358del
ENST00000638840.1:c.919+299_919+301del
ENST00000638868.1:c.*356_*358del	ENSP00000491250.1:n.*356_*358del
ENST00000639408.1:c.488-436_488-434del	ENSP00000491635.1:n.488-436_488-434del
ENST00000640017.1:c.670-436_670-434del	ENSP00000491337.1:n.670-436_670-434del
ENST00000640914.1:c.125-436_125-434del
ENST00000644903.1:c.*356_*358del MANE Select	ENSP00000495557.1:n.*356_*358del
ENST00000368089.3:c.*356_*358del	ENSP00000357068.3:n.*356_*358del
ENST00000509700.1:n.463-436_463-434del
NM_002241.4:c.*356_*358del	NP_002232.2:n.*356_*358del
NM_002241.5:c.*356_*358del MANE Select	NP_002232.2:n.*356_*358del