Canonical Allele Identifier: CA369859918

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649712G>A (hg19) ; chr7:g.150952624G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952624G>A , CM000669.2:g.150952624G>A	GRCh38
NC_000007.13:g.150649712G>A , CM000669.1:g.150649712G>A	GRCh37
NC_000007.12:g.150280645G>A	NCBI36
NG_008916.1:g.30303C>T , LRG_288:g.30303C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.656C>T
ENST00000684116.1:n.251C>T
ENST00000684241.1:n.2191C>T
ENST00000262186.10:c.1358C>T MANE Select	ENSP00000262186.5:p.Ala453Val
ENST00000330883.9:c.338C>T	ENSP00000328531.4:p.Ala113Val
ENST00000262186.9:c.1358C>T	ENSP00000262186.5:p.Ala453Val
ENST00000330883.8:c.338C>T	ENSP00000328531.4:p.Ala113Val
ENST00000430723.4:c.1010C>T	ENSP00000387657.4:p.Ala337Val
ENST00000461280.1:n.645C>T
ENST00000473610.5:n.663C>T
ENST00000532957.5:n.1581C>T
NM_000238.3:c.1358C>T , LRG_288t1:c.1358C>T	NP_000229.1:p.Ala453Val
NM_001204798.1:c.338C>T	NP_001191727.1:p.Ala113Val
NM_172056.2:c.1358C>T , LRG_288t2:c.1358C>T	NP_742053.1:p.Ala453Val
NM_172057.2:c.338C>T , LRG_288t3:c.338C>T	NP_742054.1:p.Ala113Val
XM_011516185.1:c.1058C>T	XP_011514487.1:p.Ala353Val
XM_011516186.1:c.1358C>T	XP_011514488.1:p.Ala453Val
XM_011516185.2:c.1058C>T	XP_011514487.1:p.Ala353Val
XM_011516186.3:c.1358C>T	XP_011514488.1:p.Ala453Val
XM_017012195.1:c.1208C>T	XP_016867684.1:p.Ala403Val
XM_017012196.1:c.1181C>T	XP_016867685.1:p.Ala394Val
NM_000238.4:c.1358C>T MANE Select	NP_000229.1:p.Ala453Val
NM_001204798.2:c.338C>T	NP_001191727.1:p.Ala113Val
NM_172057.3:c.338C>T	NP_742054.1:p.Ala113Val