Canonical Allele Identifier: CA10608071

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160039421_160039424dup , CM000663.2:g.160039421_160039424dup	GRCh38
NC_000001.10:g.160009211_160009214dup , CM000663.1:g.160009211_160009214dup	GRCh37
NC_000001.9:g.158275835_158275838dup	NCBI36
NG_016411.1:g.35795_35798dup

Transcript Alleles

HGVS	Amino-acid Change
NM_002241.5:c.*2016_*2019dup MANE Select	NP_002232.2:n.*2016_*2019dup
ENST00000644903.1:c.*2016_*2019dup MANE Select	ENSP00000495557.1:n.*2016_*2019dup
NM_002241.4:c.*2016_*2019dup	NP_002232.2:n.*2016_*2019dup
ENST00000368089.3:c.*2016_*2019dup	ENSP00000357068.3:n.*2016_*2019dup
ENST00000509700.2:c.671+2457_671+2460dup
ENST00000636689.1:n.95-29_95-26dup
ENST00000637644.1:c.487+2669_487+2672dup	ENSP00000490282.1:n.487+2669_487+2672dup
ENST00000638728.1:c.*2016_*2019dup	ENSP00000492619.1:n.*2016_*2019dup
ENST00000638840.1:c.2144_2147dup
ENST00000638868.1:c.*2016_*2019dup	ENSP00000491250.1:n.*2016_*2019dup
ENST00000639408.1:c.587+1125_587+1128dup	ENSP00000491635.1:n.587+1125_587+1128dup
ENST00000640017.1:c.1894_1897dup	ENSP00000491337.1:n.1894_1897dup
ENST00000640914.1:c.224+1125_224+1128dup