Canonical Allele Identifier: CA343229348

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160042297C>T , CM000663.2:g.160042297C>T	GRCh38
NC_000001.10:g.160012087C>T , CM000663.1:g.160012087C>T	GRCh37
NC_000001.9:g.158278711C>T	NCBI36
NG_016411.1:g.32875G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002241.5:c.236G>A MANE Select	NP_002232.2:p.Trp79Ter
ENST00000644903.1:c.236G>A MANE Select	ENSP00000495557.1:p.Trp79Ter
NM_002241.4:c.236G>A	NP_002232.2:p.Trp79Ter
ENST00000368089.3:c.236G>A	ENSP00000357068.3:p.Trp79Ter
ENST00000509700.2:c.208G>A
ENST00000636689.1:n.95-2949G>A
ENST00000637644.1:c.236G>A	ENSP00000490282.1:p.Trp79Ter
ENST00000638728.1:c.236G>A	ENSP00000492619.1:p.Trp79Ter
ENST00000638868.1:c.236G>A	ENSP00000491250.1:p.Trp79Ter
ENST00000639408.1:c.236G>A	ENSP00000491635.1:p.Trp79Ter
ENST00000640017.1:c.206G>A	ENSP00000491337.1:p.Trp69Ter