Canonical Allele Identifier: CA369859906

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150952618-A-G
• MyVariant Identifiers: chr7:g.150649706A>G (hg19) ; chr7:g.150952618A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952618A>G , CM000669.2:g.150952618A>G	GRCh38
NC_000007.13:g.150649706A>G , CM000669.1:g.150649706A>G	GRCh37
NC_000007.12:g.150280639A>G	NCBI36
NG_008916.1:g.30309T>C , LRG_288:g.30309T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.662T>C
ENST00000684116.1:n.257T>C
ENST00000684241.1:n.2197T>C
ENST00000262186.10:c.1364T>C MANE Select	ENSP00000262186.5:p.Val455Ala
ENST00000330883.9:c.344T>C	ENSP00000328531.4:p.Val115Ala
ENST00000262186.9:c.1364T>C	ENSP00000262186.5:p.Val455Ala
ENST00000330883.8:c.344T>C	ENSP00000328531.4:p.Val115Ala
ENST00000430723.4:c.1016T>C	ENSP00000387657.4:p.Val339Ala
ENST00000461280.1:n.651T>C
ENST00000473610.5:n.669T>C
ENST00000532957.5:n.1587T>C
NM_000238.3:c.1364T>C , LRG_288t1:c.1364T>C	NP_000229.1:p.Val455Ala
NM_001204798.1:c.344T>C	NP_001191727.1:p.Val115Ala
NM_172056.2:c.1364T>C , LRG_288t2:c.1364T>C	NP_742053.1:p.Val455Ala
NM_172057.2:c.344T>C , LRG_288t3:c.344T>C	NP_742054.1:p.Val115Ala
XM_011516185.1:c.1064T>C	XP_011514487.1:p.Val355Ala
XM_011516186.1:c.1364T>C	XP_011514488.1:p.Val455Ala
XM_011516185.2:c.1064T>C	XP_011514487.1:p.Val355Ala
XM_011516186.3:c.1364T>C	XP_011514488.1:p.Val455Ala
XM_017012195.1:c.1214T>C	XP_016867684.1:p.Val405Ala
XM_017012196.1:c.1187T>C	XP_016867685.1:p.Val396Ala
NM_000238.4:c.1364T>C MANE Select	NP_000229.1:p.Val455Ala
NM_001204798.2:c.344T>C	NP_001191727.1:p.Val115Ala
NM_172057.3:c.344T>C	NP_742054.1:p.Val115Ala