Canonical Allele Identifier: CA1752430609

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947927G= , CM000669.2:g.150947927G=	GRCh38
NC_000007.13:g.150645015G= , CM000669.1:g.150645015G=	GRCh37
NC_000007.12:g.150275948G=	NCBI36
NG_008916.1:g.35000C= , LRG_288:g.35000C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3526-49C=
ENST00000262186.10:c.2693-49C= MANE Select	ENSP00000262186.5:n.2693-49C=
ENST00000330883.9:c.1673-49C=	ENSP00000328531.4:n.1673-49C=
ENST00000262186.9:c.2693-49C=	ENSP00000262186.5:n.2693-49C=
ENST00000330883.8:c.1673-49C=	ENSP00000328531.4:n.1673-49C=
NM_000238.3:c.2693-49C= , LRG_288t1:c.2693-49C=	NP_000229.1:n.2693-49C=
NM_172057.2:c.1673-49C= , LRG_288t3:c.1673-49C=	NP_742054.1:n.1673-49C=
XM_011516185.1:c.2393-49C=	XP_011514487.1:n.2393-49C=
XM_011516186.1:c.2693-236C=	XP_011514488.1:n.2693-236C=
XM_011516185.2:c.2393-49C=	XP_011514487.1:n.2393-49C=
XM_011516186.3:c.2693-236C=	XP_011514488.1:n.2693-236C=
XM_017012195.1:c.2543-49C=	XP_016867684.1:n.2543-49C=
XM_017012196.1:c.2516-49C=	XP_016867685.1:n.2516-49C=
NM_000238.4:c.2693-49C= MANE Select	NP_000229.1:n.2693-49C=
NM_172057.3:c.1673-49C=	NP_742054.1:n.1673-49C=