Canonical Allele Identifier: CA1752428848

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947392G= , CM000669.2:g.150947392G=	GRCh38
NC_000007.13:g.150644480G= , CM000669.1:g.150644480G=	GRCh37
NC_000007.12:g.150275413G=	NCBI36
NG_008916.1:g.35535C= , LRG_288:g.35535C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3921C=
ENST00000262186.10:c.3088C= MANE Select	ENSP00000262186.5:p.Pro1030=
ENST00000330883.9:c.2068C=	ENSP00000328531.4:p.Pro690=
ENST00000262186.9:c.3088C=	ENSP00000262186.5:p.Pro1030=
ENST00000330883.8:c.2068C=	ENSP00000328531.4:p.Pro690=
NM_000238.3:c.3088C= , LRG_288t1:c.3088C=	NP_000229.1:p.Pro1030=
NM_172057.2:c.2068C= , LRG_288t3:c.2068C=	NP_742054.1:p.Pro690=
XM_011516185.1:c.2788C=	XP_011514487.1:p.Pro930=
XM_011516185.2:c.2788C=	XP_011514487.1:p.Pro930=
XM_017012195.1:c.2938C=	XP_016867684.1:p.Pro980=
XM_017012196.1:c.2911C=	XP_016867685.1:p.Pro971=
NM_000238.4:c.3088C= MANE Select	NP_000229.1:p.Pro1030=
NM_172057.3:c.2068C=	NP_742054.1:p.Pro690=