Canonical Allele Identifier: CA1752430399

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947818C= , CM000669.2:g.150947818C=	GRCh38
NC_000007.13:g.150644906C= , CM000669.1:g.150644906C=	GRCh37
NC_000007.12:g.150275839C=	NCBI36
NG_008916.1:g.35109G= , LRG_288:g.35109G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3586G=
ENST00000262186.10:c.2753G= MANE Select	ENSP00000262186.5:p.Ser918=
ENST00000330883.9:c.1733G=	ENSP00000328531.4:p.Ser578=
ENST00000262186.9:c.2753G=	ENSP00000262186.5:p.Ser918=
ENST00000330883.8:c.1733G=	ENSP00000328531.4:p.Ser578=
NM_000238.3:c.2753G= , LRG_288t1:c.2753G=	NP_000229.1:p.Ser918=
NM_172057.2:c.1733G= , LRG_288t3:c.1733G=	NP_742054.1:p.Ser578=
XM_011516185.1:c.2453G=	XP_011514487.1:p.Ser818=
XM_011516186.1:c.2693-127G=	XP_011514488.1:n.2693-127G=
XM_011516185.2:c.2453G=	XP_011514487.1:p.Ser818=
XM_011516186.3:c.2693-127G=	XP_011514488.1:n.2693-127G=
XM_017012195.1:c.2603G=	XP_016867684.1:p.Ser868=
XM_017012196.1:c.2576G=	XP_016867685.1:p.Ser859=
NM_000238.4:c.2753G= MANE Select	NP_000229.1:p.Ser918=
NM_172057.3:c.1733G=	NP_742054.1:p.Ser578=