Canonical Allele Identifier: CA1752431423

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948487C= , CM000669.2:g.150948487C=	GRCh38
NC_000007.13:g.150645575C= , CM000669.1:g.150645575C=	GRCh37
NC_000007.12:g.150276508C=	NCBI36
NG_008916.1:g.34440G= , LRG_288:g.34440G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3482G=
ENST00000262186.10:c.2649G= MANE Select	ENSP00000262186.5:p.Arg883=
ENST00000330883.9:c.1629G=	ENSP00000328531.4:p.Arg543=
ENST00000262186.9:c.2649G=	ENSP00000262186.5:p.Arg883=
ENST00000330883.8:c.1629G=	ENSP00000328531.4:p.Arg543=
NM_000238.3:c.2649G= , LRG_288t1:c.2649G=	NP_000229.1:p.Arg883=
NM_172057.2:c.1629G= , LRG_288t3:c.1629G=	NP_742054.1:p.Arg543=
XM_011516185.1:c.2349G=	XP_011514487.1:p.Arg783=
XM_011516186.1:c.2649G=	XP_011514488.1:p.Arg883=
XM_011516185.2:c.2349G=	XP_011514487.1:p.Arg783=
XM_011516186.3:c.2649G=	XP_011514488.1:p.Arg883=
XM_017012195.1:c.2499G=	XP_016867684.1:p.Arg833=
XM_017012196.1:c.2472G=	XP_016867685.1:p.Arg824=
NM_000238.4:c.2649G= MANE Select	NP_000229.1:p.Arg883=
NM_172057.3:c.1629G=	NP_742054.1:p.Arg543=