Canonical Allele Identifier: CA1752441182

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974879C= , CM000669.2:g.150974879C=	GRCh38
NC_000007.13:g.150671967C= , CM000669.1:g.150671967C=	GRCh37
NC_000007.12:g.150302900C=	NCBI36
NG_008916.1:g.8048G= , LRG_288:g.8048G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.139G= MANE Select	ENSP00000262186.5:p.Gly47=
ENST00000262186.9:c.139G=	ENSP00000262186.5:p.Gly47=
ENST00000430723.4:c.-39G=	ENSP00000387657.4:n.-39G=
ENST00000532957.5:n.362G=
NM_000238.3:c.139G= , LRG_288t1:c.139G=	NP_000229.1:p.Gly47=
NM_172056.2:c.139G= , LRG_288t2:c.139G=	NP_742053.1:p.Gly47=
XM_011516186.1:c.139G=	XP_011514488.1:p.Gly47=
XM_011516186.3:c.139G=	XP_011514488.1:p.Gly47=
XM_017012196.1:c.-39G=	XP_016867685.1:n.-39G=
NM_000238.4:c.139G= MANE Select	NP_000229.1:p.Gly47=