Canonical Allele Identifier: CA1752417155

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957571C= , CM000669.2:g.150957571C=	GRCh38
NC_000007.13:g.150654659C= , CM000669.1:g.150654659C=	GRCh37
NC_000007.12:g.150285592C=	NCBI36
NG_008916.1:g.25356G= , LRG_288:g.25356G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1750-69G=
ENST00000262186.10:c.917-69G= MANE Select	ENSP00000262186.5:n.917-69G=
ENST00000262186.9:c.917-69G=	ENSP00000262186.5:n.917-69G=
ENST00000430723.4:c.569-69G=	ENSP00000387657.4:n.569-69G=
ENST00000532957.5:n.1140-69G=
NM_000238.3:c.917-69G= , LRG_288t1:c.917-69G=	NP_000229.1:n.917-69G=
NM_172056.2:c.917-69G= , LRG_288t2:c.917-69G=	NP_742053.1:n.917-69G=
XM_011516185.1:c.617-69G=	XP_011514487.1:n.617-69G=
XM_011516186.1:c.917-69G=	XP_011514488.1:n.917-69G=
XM_011516185.2:c.617-69G=	XP_011514487.1:n.617-69G=
XM_011516186.3:c.917-69G=	XP_011514488.1:n.917-69G=
XM_017012195.1:c.767-69G=	XP_016867684.1:n.767-69G=
XM_017012196.1:c.740-69G=	XP_016867685.1:n.740-69G=
NM_000238.4:c.917-69G= MANE Select	NP_000229.1:n.917-69G=