Canonical Allele Identifier: CA1752461929

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974744G= , CM000669.2:g.150974744G=	GRCh38
NC_000007.13:g.150671832G= , CM000669.1:g.150671832G=	GRCh37
NC_000007.12:g.150302765G=	NCBI36
NG_008916.1:g.8183C= , LRG_288:g.8183C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.274C= MANE Select	ENSP00000262186.5:p.Arg92=
ENST00000262186.9:c.274C=	ENSP00000262186.5:p.Arg92=
ENST00000430723.4:c.97C=	ENSP00000387657.4:p.Arg33=
ENST00000532957.5:n.497C=
NM_000238.3:c.274C= , LRG_288t1:c.274C=	NP_000229.1:p.Arg92=
NM_172056.2:c.274C= , LRG_288t2:c.274C=	NP_742053.1:p.Arg92=
XM_011516186.1:c.274C=	XP_011514488.1:p.Arg92=
XM_011516186.3:c.274C=	XP_011514488.1:p.Arg92=
XM_017012196.1:c.97C=	XP_016867685.1:p.Arg33=
NM_000238.4:c.274C= MANE Select	NP_000229.1:p.Arg92=