Canonical Allele Identifier: CA1752461898

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974741T= , CM000669.2:g.150974741T=	GRCh38
NC_000007.13:g.150671829T= , CM000669.1:g.150671829T=	GRCh37
NC_000007.12:g.150302762T=	NCBI36
NG_008916.1:g.8186A= , LRG_288:g.8186A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.277A= MANE Select	ENSP00000262186.5:p.Lys93=
ENST00000262186.9:c.277A=	ENSP00000262186.5:p.Lys93=
ENST00000430723.4:c.100A=	ENSP00000387657.4:p.Lys34=
ENST00000532957.5:n.500A=
NM_000238.3:c.277A= , LRG_288t1:c.277A=	NP_000229.1:p.Lys93=
NM_172056.2:c.277A= , LRG_288t2:c.277A=	NP_742053.1:p.Lys93=
XM_011516186.1:c.277A=	XP_011514488.1:p.Lys93=
XM_011516186.3:c.277A=	XP_011514488.1:p.Lys93=
XM_017012196.1:c.100A=	XP_016867685.1:p.Lys34=
NM_000238.4:c.277A= MANE Select	NP_000229.1:p.Lys93=