Canonical Allele Identifier: CA1752417681

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958059C= , CM000669.2:g.150958059C=	GRCh38
NC_000007.13:g.150655147C= , CM000669.1:g.150655147C=	GRCh37
NC_000007.12:g.150286080C=	NCBI36
NG_008916.1:g.24868G= , LRG_288:g.24868G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000238.4:c.916G= MANE Select	NP_000229.1:p.Gly306=
ENST00000262186.10:c.916G= MANE Select	ENSP00000262186.5:p.Gly306=
NM_000238.3:c.916G= , LRG_288t1:c.916G=	NP_000229.1:p.Gly306=
NM_172056.2:c.916G= , LRG_288t2:c.916G=	NP_742053.1:p.Gly306=
ENST00000262186.9:c.916G=	ENSP00000262186.5:p.Gly306=
ENST00000430723.4:c.568G=	ENSP00000387657.4:p.Gly190=
ENST00000532957.5:n.1139G=
ENST00000684241.1:n.1749G=
XM_011516185.1:c.616G=	XP_011514487.1:p.Gly206=
XM_011516185.2:c.616G=	XP_011514487.1:p.Gly206=
XM_011516186.1:c.916G=	XP_011514488.1:p.Gly306=
XM_011516186.3:c.916G=	XP_011514488.1:p.Gly306=
XM_017012195.1:c.766G=	XP_016867684.1:p.Gly256=
XM_017012196.1:c.739G=	XP_016867685.1:p.Gly247=