Canonical Allele Identifier: CA1752430456

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947840C= , CM000669.2:g.150947840C=	GRCh38
NC_000007.13:g.150644928C= , CM000669.1:g.150644928C=	GRCh37
NC_000007.12:g.150275861C=	NCBI36
NG_008916.1:g.35087G= , LRG_288:g.35087G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3564G=
ENST00000262186.10:c.2731G= MANE Select	ENSP00000262186.5:p.Gly911=
ENST00000330883.9:c.1711G=	ENSP00000328531.4:p.Gly571=
ENST00000262186.9:c.2731G=	ENSP00000262186.5:p.Gly911=
ENST00000330883.8:c.1711G=	ENSP00000328531.4:p.Gly571=
NM_000238.3:c.2731G= , LRG_288t1:c.2731G=	NP_000229.1:p.Gly911=
NM_172057.2:c.1711G= , LRG_288t3:c.1711G=	NP_742054.1:p.Gly571=
XM_011516185.1:c.2431G=	XP_011514487.1:p.Gly811=
XM_011516186.1:c.2693-149G=	XP_011514488.1:n.2693-149G=
XM_011516185.2:c.2431G=	XP_011514487.1:p.Gly811=
XM_011516186.3:c.2693-149G=	XP_011514488.1:n.2693-149G=
XM_017012195.1:c.2581G=	XP_016867684.1:p.Gly861=
XM_017012196.1:c.2554G=	XP_016867685.1:p.Gly852=
NM_000238.4:c.2731G= MANE Select	NP_000229.1:p.Gly911=
NM_172057.3:c.1711G=	NP_742054.1:p.Gly571=