Canonical Allele Identifier: CA1752417085

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957534A= , CM000669.2:g.150957534A=	GRCh38
NC_000007.13:g.150654622A= , CM000669.1:g.150654622A=	GRCh37
NC_000007.12:g.150285555A=	NCBI36
NG_008916.1:g.25393T= , LRG_288:g.25393T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1750-32T=
ENST00000262186.10:c.917-32T= MANE Select	ENSP00000262186.5:n.917-32T=
ENST00000262186.9:c.917-32T=	ENSP00000262186.5:n.917-32T=
ENST00000430723.4:c.569-32T=	ENSP00000387657.4:n.569-32T=
ENST00000532957.5:n.1140-32T=
NM_000238.3:c.917-32T= , LRG_288t1:c.917-32T=	NP_000229.1:n.917-32T=
NM_172056.2:c.917-32T= , LRG_288t2:c.917-32T=	NP_742053.1:n.917-32T=
XM_011516185.1:c.617-32T=	XP_011514487.1:n.617-32T=
XM_011516186.1:c.917-32T=	XP_011514488.1:n.917-32T=
XM_011516185.2:c.617-32T=	XP_011514487.1:n.617-32T=
XM_011516186.3:c.917-32T=	XP_011514488.1:n.917-32T=
XM_017012195.1:c.767-32T=	XP_016867684.1:n.767-32T=
XM_017012196.1:c.740-32T=	XP_016867685.1:n.740-32T=
NM_000238.4:c.917-32T= MANE Select	NP_000229.1:n.917-32T=