Canonical Allele Identifier: CA1752462227

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974797G= , CM000669.2:g.150974797G=	GRCh38
NC_000007.13:g.150671885G= , CM000669.1:g.150671885G=	GRCh37
NC_000007.12:g.150302818G=	NCBI36
NG_008916.1:g.8130C= , LRG_288:g.8130C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000238.4:c.221C= MANE Select	NP_000229.1:p.Thr74=
ENST00000262186.10:c.221C= MANE Select	ENSP00000262186.5:p.Thr74=
NM_000238.3:c.221C= , LRG_288t1:c.221C=	NP_000229.1:p.Thr74=
NM_172056.2:c.221C= , LRG_288t2:c.221C=	NP_742053.1:p.Thr74=
ENST00000262186.9:c.221C=	ENSP00000262186.5:p.Thr74=
ENST00000430723.4:c.44C=	ENSP00000387657.4:p.Thr15=
ENST00000532957.5:n.444C=
XM_011516186.1:c.221C=	XP_011514488.1:p.Thr74=
XM_011516186.3:c.221C=	XP_011514488.1:p.Thr74=
XM_017012196.1:c.44C=	XP_016867685.1:p.Thr15=