Canonical Allele Identifier: CA1752441101

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974865C= , CM000669.2:g.150974865C=	GRCh38
NC_000007.13:g.150671953C= , CM000669.1:g.150671953C=	GRCh37
NC_000007.12:g.150302886C=	NCBI36
NG_008916.1:g.8062G= , LRG_288:g.8062G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.153G= MANE Select	ENSP00000262186.5:p.Leu51=
ENST00000262186.9:c.153G=	ENSP00000262186.5:p.Leu51=
ENST00000430723.4:c.-25G=	ENSP00000387657.4:n.-25G=
ENST00000532957.5:n.376G=
NM_000238.3:c.153G= , LRG_288t1:c.153G=	NP_000229.1:p.Leu51=
NM_172056.2:c.153G= , LRG_288t2:c.153G=	NP_742053.1:p.Leu51=
XM_011516186.1:c.153G=	XP_011514488.1:p.Leu51=
XM_011516186.3:c.153G=	XP_011514488.1:p.Leu51=
XM_017012196.1:c.-25G=	XP_016867685.1:n.-25G=
NM_000238.4:c.153G= MANE Select	NP_000229.1:p.Leu51=