Canonical Allele Identifier: CA1752433427

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950241C= , CM000669.2:g.150950241C=	GRCh38
NC_000007.13:g.150647329C= , CM000669.1:g.150647329C=	GRCh37
NC_000007.12:g.150278262C=	NCBI36
NG_008916.1:g.32686G= , LRG_288:g.32686G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1623G=
ENST00000684241.1:n.3158G=
ENST00000262186.10:c.2325G= MANE Select	ENSP00000262186.5:p.Leu775=
ENST00000330883.9:c.1305G=	ENSP00000328531.4:p.Leu435=
ENST00000262186.9:c.2325G=	ENSP00000262186.5:p.Leu775=
ENST00000330883.8:c.1305G=	ENSP00000328531.4:p.Leu435=
ENST00000430723.4:c.1977G=	ENSP00000387657.4:p.Leu659=
ENST00000461280.1:n.1612G=
ENST00000473610.5:n.1957G=
ENST00000532957.5:n.2548G=
NM_000238.3:c.2325G= , LRG_288t1:c.2325G=	NP_000229.1:p.Leu775=
NM_001204798.1:c.1305G=	NP_001191727.1:p.Leu435=
NM_172056.2:c.2325G= , LRG_288t2:c.2325G=	NP_742053.1:p.Leu775=
NM_172057.2:c.1305G= , LRG_288t3:c.1305G=	NP_742054.1:p.Leu435=
XM_011516185.1:c.2025G=	XP_011514487.1:p.Leu675=
XM_011516186.1:c.2325G=	XP_011514488.1:p.Leu775=
XM_011516185.2:c.2025G=	XP_011514487.1:p.Leu675=
XM_011516186.3:c.2325G=	XP_011514488.1:p.Leu775=
XM_017012195.1:c.2175G=	XP_016867684.1:p.Leu725=
XM_017012196.1:c.2148G=	XP_016867685.1:p.Leu716=
NM_000238.4:c.2325G= MANE Select	NP_000229.1:p.Leu775=
NM_001204798.2:c.1305G=	NP_001191727.1:p.Leu435=
NM_172057.3:c.1305G=	NP_742054.1:p.Leu435=