Canonical Allele Identifier: CA1752441868

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150975039A= , CM000669.2:g.150975039A=	GRCh38
NC_000007.13:g.150672127A= , CM000669.1:g.150672127A=	GRCh37
NC_000007.12:g.150303060A=	NCBI36
NG_008916.1:g.7888T= , LRG_288:g.7888T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.77-98T= MANE Select	ENSP00000262186.5:n.77-98T=
ENST00000262186.9:c.77-98T=	ENSP00000262186.5:n.77-98T=
ENST00000430723.4:c.-101-98T=	ENSP00000387657.4:n.-101-98T=
ENST00000532957.5:n.300-98T=
NM_000238.3:c.77-98T= , LRG_288t1:c.77-98T=	NP_000229.1:n.77-98T=
NM_172056.2:c.77-98T= , LRG_288t2:c.77-98T=	NP_742053.1:n.77-98T=
XM_011516186.1:c.77-98T=	XP_011514488.1:n.77-98T=
XM_011516186.3:c.77-98T=	XP_011514488.1:n.77-98T=
XM_017012196.1:c.-116T=	XP_016867685.1:n.-116T=
NM_000238.4:c.77-98T= MANE Select	NP_000229.1:n.77-98T=