Canonical Allele Identifier: CA1752428078

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947138G= , CM000669.2:g.150947138G=	GRCh38
NC_000007.13:g.150644226G= , CM000669.1:g.150644226G=	GRCh37
NC_000007.12:g.150275159G=	NCBI36
NG_008916.1:g.35789C= , LRG_288:g.35789C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3986-84C=
ENST00000262186.10:c.3153-84C= MANE Select	ENSP00000262186.5:n.3153-84C=
ENST00000330883.9:c.2133-84C=	ENSP00000328531.4:n.2133-84C=
ENST00000262186.9:c.3153-84C=	ENSP00000262186.5:n.3153-84C=
ENST00000330883.8:c.2133-84C=	ENSP00000328531.4:n.2133-84C=
NM_000238.3:c.3153-84C= , LRG_288t1:c.3153-84C=	NP_000229.1:n.3153-84C=
NM_172057.2:c.2133-84C= , LRG_288t3:c.2133-84C=	NP_742054.1:n.2133-84C=
XM_011516185.1:c.2853-84C=	XP_011514487.1:n.2853-84C=
XM_011516185.2:c.2853-84C=	XP_011514487.1:n.2853-84C=
XM_017012195.1:c.3003-84C=	XP_016867684.1:n.3003-84C=
XM_017012196.1:c.2976-84C=	XP_016867685.1:n.2976-84C=
NM_000238.4:c.3153-84C= MANE Select	NP_000229.1:n.3153-84C=
NM_172057.3:c.2133-84C=	NP_742054.1:n.2133-84C=