Canonical Allele Identifier: CA1752446512

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150977899C= , CM000669.2:g.150977899C=	GRCh38
NC_000007.13:g.150674987C= , CM000669.1:g.150674987C=	GRCh37
NC_000007.12:g.150305920C=	NCBI36
NG_008916.1:g.5028G= , LRG_288:g.5028G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.15G= MANE Select	ENSP00000262186.5:p.Arg5=
ENST00000262186.9:c.15G=	ENSP00000262186.5:p.Arg5=
ENST00000430723.4:c.-163G=	ENSP00000387657.4:n.-163G=
ENST00000532957.5:n.238G=
NM_000238.3:c.15G= , LRG_288t1:c.15G=	NP_000229.1:p.Arg5=
NM_172056.2:c.15G= , LRG_288t2:c.15G=	NP_742053.1:p.Arg5=
XM_011516186.1:c.15G=	XP_011514488.1:p.Arg5=
XM_011516186.3:c.15G=	XP_011514488.1:p.Arg5=
NM_000238.4:c.15G= MANE Select	NP_000229.1:p.Arg5=