Canonical Allele Identifier: CA1752431309

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948455C= , CM000669.2:g.150948455C=	GRCh38
NC_000007.13:g.150645543C= , CM000669.1:g.150645543C=	GRCh37
NC_000007.12:g.150276476C=	NCBI36
NG_008916.1:g.34472G= , LRG_288:g.34472G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3514G=
ENST00000262186.10:c.2681G= MANE Select	ENSP00000262186.5:p.Arg894=
ENST00000330883.9:c.1661G=	ENSP00000328531.4:p.Arg554=
ENST00000262186.9:c.2681G=	ENSP00000262186.5:p.Arg894=
ENST00000330883.8:c.1661G=	ENSP00000328531.4:p.Arg554=
NM_000238.3:c.2681G= , LRG_288t1:c.2681G=	NP_000229.1:p.Arg894=
NM_172057.2:c.1661G= , LRG_288t3:c.1661G=	NP_742054.1:p.Arg554=
XM_011516185.1:c.2381G=	XP_011514487.1:p.Arg794=
XM_011516186.1:c.2681G=	XP_011514488.1:p.Arg894=
XM_011516185.2:c.2381G=	XP_011514487.1:p.Arg794=
XM_011516186.3:c.2681G=	XP_011514488.1:p.Arg894=
XM_017012195.1:c.2531G=	XP_016867684.1:p.Arg844=
XM_017012196.1:c.2504G=	XP_016867685.1:p.Arg835=
NM_000238.4:c.2681G= MANE Select	NP_000229.1:p.Arg894=
NM_172057.3:c.1661G=	NP_742054.1:p.Arg554=