Canonical Allele Identifier: CA1752430393

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947813G= , CM000669.2:g.150947813G=	GRCh38
NC_000007.13:g.150644901G= , CM000669.1:g.150644901G=	GRCh37
NC_000007.12:g.150275834G=	NCBI36
NG_008916.1:g.35114C= , LRG_288:g.35114C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3591C=
ENST00000262186.10:c.2758C= MANE Select	ENSP00000262186.5:p.Arg920=
ENST00000330883.9:c.1738C=	ENSP00000328531.4:p.Arg580=
ENST00000262186.9:c.2758C=	ENSP00000262186.5:p.Arg920=
ENST00000330883.8:c.1738C=	ENSP00000328531.4:p.Arg580=
NM_000238.3:c.2758C= , LRG_288t1:c.2758C=	NP_000229.1:p.Arg920=
NM_172057.2:c.1738C= , LRG_288t3:c.1738C=	NP_742054.1:p.Arg580=
XM_011516185.1:c.2458C=	XP_011514487.1:p.Arg820=
XM_011516186.1:c.2693-122C=	XP_011514488.1:n.2693-122C=
XM_011516185.2:c.2458C=	XP_011514487.1:p.Arg820=
XM_011516186.3:c.2693-122C=	XP_011514488.1:n.2693-122C=
XM_017012195.1:c.2608C=	XP_016867684.1:p.Arg870=
XM_017012196.1:c.2581C=	XP_016867685.1:p.Arg861=
NM_000238.4:c.2758C= MANE Select	NP_000229.1:p.Arg920=
NM_172057.3:c.1738C=	NP_742054.1:p.Arg580=