Canonical Allele Identifier: CA1752431444

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948496G= , CM000669.2:g.150948496G=	GRCh38
NC_000007.13:g.150645584G= , CM000669.1:g.150645584G=	GRCh37
NC_000007.12:g.150276517G=	NCBI36
NG_008916.1:g.34431C= , LRG_288:g.34431C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3473C=
ENST00000262186.10:c.2640C= MANE Select	ENSP00000262186.5:p.Gly880=
ENST00000330883.9:c.1620C=	ENSP00000328531.4:p.Gly540=
ENST00000262186.9:c.2640C=	ENSP00000262186.5:p.Gly880=
ENST00000330883.8:c.1620C=	ENSP00000328531.4:p.Gly540=
NM_000238.3:c.2640C= , LRG_288t1:c.2640C=	NP_000229.1:p.Gly880=
NM_172057.2:c.1620C= , LRG_288t3:c.1620C=	NP_742054.1:p.Gly540=
XM_011516185.1:c.2340C=	XP_011514487.1:p.Gly780=
XM_011516186.1:c.2640C=	XP_011514488.1:p.Gly880=
XM_011516185.2:c.2340C=	XP_011514487.1:p.Gly780=
XM_011516186.3:c.2640C=	XP_011514488.1:p.Gly880=
XM_017012195.1:c.2490C=	XP_016867684.1:p.Gly830=
XM_017012196.1:c.2463C=	XP_016867685.1:p.Gly821=
NM_000238.4:c.2640C= MANE Select	NP_000229.1:p.Gly880=
NM_172057.3:c.1620C=	NP_742054.1:p.Gly540=