Canonical Allele Identifier: CA1752442139

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150975161T= , CM000669.2:g.150975161T=	GRCh38
NC_000007.13:g.150672249T= , CM000669.1:g.150672249T=	GRCh37
NC_000007.12:g.150303182T=	NCBI36
NG_008916.1:g.7766A= , LRG_288:g.7766A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.77-220A= MANE Select	ENSP00000262186.5:n.77-220A=
ENST00000262186.9:c.77-220A=	ENSP00000262186.5:n.77-220A=
ENST00000430723.4:c.-101-220A=	ENSP00000387657.4:n.-101-220A=
ENST00000532957.5:n.300-220A=
NM_000238.3:c.77-220A= , LRG_288t1:c.77-220A=	NP_000229.1:n.77-220A=
NM_172056.2:c.77-220A= , LRG_288t2:c.77-220A=	NP_742053.1:n.77-220A=
XM_011516186.1:c.77-220A=	XP_011514488.1:n.77-220A=
XM_011516186.3:c.77-220A=	XP_011514488.1:n.77-220A=
NM_000238.4:c.77-220A= MANE Select	NP_000229.1:n.77-220A=