Canonical Allele Identifier: CA1752441818

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150975001C= , CM000669.2:g.150975001C=	GRCh38
NC_000007.13:g.150672089C= , CM000669.1:g.150672089C=	GRCh37
NC_000007.12:g.150303022C=	NCBI36
NG_008916.1:g.7926G= , LRG_288:g.7926G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.77-60G= MANE Select	ENSP00000262186.5:n.77-60G=
ENST00000262186.9:c.77-60G=	ENSP00000262186.5:n.77-60G=
ENST00000430723.4:c.-101-60G=	ENSP00000387657.4:n.-101-60G=
ENST00000532957.5:n.300-60G=
NM_000238.3:c.77-60G= , LRG_288t1:c.77-60G=	NP_000229.1:n.77-60G=
NM_172056.2:c.77-60G= , LRG_288t2:c.77-60G=	NP_742053.1:n.77-60G=
XM_011516186.1:c.77-60G=	XP_011514488.1:n.77-60G=
XM_011516186.3:c.77-60G=	XP_011514488.1:n.77-60G=
XM_017012196.1:c.-102+24G=	XP_016867685.1:n.-102+24G=
NM_000238.4:c.77-60G= MANE Select	NP_000229.1:n.77-60G=