Canonical Allele Identifier: CA1752429633

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947590C= , CM000669.2:g.150947590C=	GRCh38
NC_000007.13:g.150644678C= , CM000669.1:g.150644678C=	GRCh37
NC_000007.12:g.150275611C=	NCBI36
NG_008916.1:g.35337G= , LRG_288:g.35337G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3798+16G=
ENST00000262186.10:c.2965+16G= MANE Select	ENSP00000262186.5:n.2965+16G=
ENST00000330883.9:c.1945+16G=	ENSP00000328531.4:n.1945+16G=
ENST00000262186.9:c.2965+16G=	ENSP00000262186.5:n.2965+16G=
ENST00000330883.8:c.1945+16G=	ENSP00000328531.4:n.1945+16G=
NM_000238.3:c.2965+16G= , LRG_288t1:c.2965+16G=	NP_000229.1:n.2965+16G=
NM_172057.2:c.1945+16G= , LRG_288t3:c.1945+16G=	NP_742054.1:n.1945+16G=
XM_011516185.1:c.2665+16G=	XP_011514487.1:n.2665+16G=
XM_011516186.1:c.*45+16G=	XP_011514488.1:n.*45+16G=
XM_011516185.2:c.2665+16G=	XP_011514487.1:n.2665+16G=
XM_011516186.3:c.*45+16G=	XP_011514488.1:n.*45+16G=
XM_017012195.1:c.2815+16G=	XP_016867684.1:n.2815+16G=
XM_017012196.1:c.2788+16G=	XP_016867685.1:n.2788+16G=
NM_000238.4:c.2965+16G= MANE Select	NP_000229.1:n.2965+16G=
NM_172057.3:c.1945+16G=	NP_742054.1:n.1945+16G=