Canonical Allele Identifier: CA1752427467

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150946927G= , CM000669.2:g.150946927G=	GRCh38
NC_000007.13:g.150644015G= , CM000669.1:g.150644015G=	GRCh37
NC_000007.12:g.150274948G=	NCBI36
NG_008916.1:g.36000C= , LRG_288:g.36000C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.4113C=
ENST00000262186.10:c.3280C= MANE Select	ENSP00000262186.5:p.Leu1094=
ENST00000330883.9:c.2260C=	ENSP00000328531.4:p.Leu754=
ENST00000262186.9:c.3280C=	ENSP00000262186.5:p.Leu1094=
ENST00000330883.8:c.2260C=	ENSP00000328531.4:p.Leu754=
NM_000238.3:c.3280C= , LRG_288t1:c.3280C=	NP_000229.1:p.Leu1094=
NM_172057.2:c.2260C= , LRG_288t3:c.2260C=	NP_742054.1:p.Leu754=
XM_011516185.1:c.2980C=	XP_011514487.1:p.Leu994=
XM_011516185.2:c.2980C=	XP_011514487.1:p.Leu994=
XM_017012195.1:c.3130C=	XP_016867684.1:p.Leu1044=
XM_017012196.1:c.3103C=	XP_016867685.1:p.Leu1035=
NM_000238.4:c.3280C= MANE Select	NP_000229.1:p.Leu1094=
NM_172057.3:c.2260C=	NP_742054.1:p.Leu754=