Canonical Allele Identifier: CA1752418284

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958278C= , CM000669.2:g.150958278C=	GRCh38
NC_000007.13:g.150655366C= , CM000669.1:g.150655366C=	GRCh37
NC_000007.12:g.150286299C=	NCBI36
NG_008916.1:g.24649G= , LRG_288:g.24649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1530G=
ENST00000262186.10:c.697G= MANE Select	ENSP00000262186.5:p.Ala233=
ENST00000262186.9:c.697G=	ENSP00000262186.5:p.Ala233=
ENST00000430723.4:c.349G=	ENSP00000387657.4:p.Ala117=
ENST00000532957.5:n.920G=
NM_000238.3:c.697G= , LRG_288t1:c.697G=	NP_000229.1:p.Ala233=
NM_172056.2:c.697G= , LRG_288t2:c.697G=	NP_742053.1:p.Ala233=
XM_011516185.1:c.397G=	XP_011514487.1:p.Ala133=
XM_011516186.1:c.697G=	XP_011514488.1:p.Ala233=
XM_011516185.2:c.397G=	XP_011514487.1:p.Ala133=
XM_011516186.3:c.697G=	XP_011514488.1:p.Ala233=
XM_017012195.1:c.547G=	XP_016867684.1:p.Ala183=
XM_017012196.1:c.520G=	XP_016867685.1:p.Ala174=
NM_000238.4:c.697G= MANE Select	NP_000229.1:p.Ala233=