Canonical Allele Identifier: CA1752418269

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958273C= , CM000669.2:g.150958273C=	GRCh38
NC_000007.13:g.150655361C= , CM000669.1:g.150655361C=	GRCh37
NC_000007.12:g.150286294C=	NCBI36
NG_008916.1:g.24654G= , LRG_288:g.24654G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1535G=
ENST00000262186.10:c.702G= MANE Select	ENSP00000262186.5:p.Leu234=
ENST00000262186.9:c.702G=	ENSP00000262186.5:p.Leu234=
ENST00000430723.4:c.354G=	ENSP00000387657.4:p.Leu118=
ENST00000532957.5:n.925G=
NM_000238.3:c.702G= , LRG_288t1:c.702G=	NP_000229.1:p.Leu234=
NM_172056.2:c.702G= , LRG_288t2:c.702G=	NP_742053.1:p.Leu234=
XM_011516185.1:c.402G=	XP_011514487.1:p.Leu134=
XM_011516186.1:c.702G=	XP_011514488.1:p.Leu234=
XM_011516185.2:c.402G=	XP_011514487.1:p.Leu134=
XM_011516186.3:c.702G=	XP_011514488.1:p.Leu234=
XM_017012195.1:c.552G=	XP_016867684.1:p.Leu184=
XM_017012196.1:c.525G=	XP_016867685.1:p.Leu175=
NM_000238.4:c.702G= MANE Select	NP_000229.1:p.Leu234=