Canonical Allele Identifier: CA1752429873

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947645C= , CM000669.2:g.150947645C=	GRCh38
NC_000007.13:g.150644733C= , CM000669.1:g.150644733C=	GRCh37
NC_000007.12:g.150275666C=	NCBI36
NG_008916.1:g.35282G= , LRG_288:g.35282G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3759G=
ENST00000262186.10:c.2926G= MANE Select	ENSP00000262186.5:p.Asp976=
ENST00000330883.9:c.1906G=	ENSP00000328531.4:p.Asp636=
ENST00000262186.9:c.2926G=	ENSP00000262186.5:p.Asp976=
ENST00000330883.8:c.1906G=	ENSP00000328531.4:p.Asp636=
NM_000238.3:c.2926G= , LRG_288t1:c.2926G=	NP_000229.1:p.Asp976=
NM_172057.2:c.1906G= , LRG_288t3:c.1906G=	NP_742054.1:p.Asp636=
XM_011516185.1:c.2626G=	XP_011514487.1:p.Asp876=
XM_011516186.1:c.*6G=	XP_011514488.1:n.*6G=
XM_011516185.2:c.2626G=	XP_011514487.1:p.Asp876=
XM_011516186.3:c.*6G=	XP_011514488.1:n.*6G=
XM_017012195.1:c.2776G=	XP_016867684.1:p.Asp926=
XM_017012196.1:c.2749G=	XP_016867685.1:p.Asp917=
NM_000238.4:c.2926G= MANE Select	NP_000229.1:p.Asp976=
NM_172057.3:c.1906G=	NP_742054.1:p.Asp636=