Canonical Allele Identifier: CA1752461569

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974664C= , CM000669.2:g.150974664C=	GRCh38
NC_000007.13:g.150671752C= , CM000669.1:g.150671752C=	GRCh37
NC_000007.12:g.150302685C=	NCBI36
NG_008916.1:g.8263G= , LRG_288:g.8263G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.307+47G= MANE Select	ENSP00000262186.5:n.307+47G=
ENST00000262186.9:c.307+47G=	ENSP00000262186.5:n.307+47G=
ENST00000430723.4:c.130+47G=	ENSP00000387657.4:n.130+47G=
ENST00000532957.5:n.530+47G=
NM_000238.3:c.307+47G= , LRG_288t1:c.307+47G=	NP_000229.1:n.307+47G=
NM_172056.2:c.307+47G= , LRG_288t2:c.307+47G=	NP_742053.1:n.307+47G=
XM_011516186.1:c.307+47G=	XP_011514488.1:n.307+47G=
XM_011516186.3:c.307+47G=	XP_011514488.1:n.307+47G=
XM_017012196.1:c.130+47G=	XP_016867685.1:n.130+47G=
NM_000238.4:c.307+47G= MANE Select	NP_000229.1:n.307+47G=