Canonical Allele Identifier: CA1752416896

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957458C= , CM000669.2:g.150957458C=	GRCh38
NC_000007.13:g.150654546C= , CM000669.1:g.150654546C=	GRCh37
NC_000007.12:g.150285479C=	NCBI36
NG_008916.1:g.25469G= , LRG_288:g.25469G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1794G=
ENST00000262186.10:c.961G= MANE Select	ENSP00000262186.5:p.Asp321=
ENST00000262186.9:c.961G=	ENSP00000262186.5:p.Asp321=
ENST00000430723.4:c.613G=	ENSP00000387657.4:p.Asp205=
ENST00000532957.5:n.1184G=
NM_000238.3:c.961G= , LRG_288t1:c.961G=	NP_000229.1:p.Asp321=
NM_172056.2:c.961G= , LRG_288t2:c.961G=	NP_742053.1:p.Asp321=
XM_011516185.1:c.661G=	XP_011514487.1:p.Asp221=
XM_011516186.1:c.961G=	XP_011514488.1:p.Asp321=
XM_011516185.2:c.661G=	XP_011514487.1:p.Asp221=
XM_011516186.3:c.961G=	XP_011514488.1:p.Asp321=
XM_017012195.1:c.811G=	XP_016867684.1:p.Asp271=
XM_017012196.1:c.784G=	XP_016867685.1:p.Asp262=
NM_000238.4:c.961G= MANE Select	NP_000229.1:p.Asp321=