Canonical Allele Identifier: CA1752430569

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947893G= , CM000669.2:g.150947893G=	GRCh38
NC_000007.13:g.150644981G= , CM000669.1:g.150644981G=	GRCh37
NC_000007.12:g.150275914G=	NCBI36
NG_008916.1:g.35034C= , LRG_288:g.35034C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3526-15C=
ENST00000262186.10:c.2693-15C= MANE Select	ENSP00000262186.5:n.2693-15C=
ENST00000330883.9:c.1673-15C=	ENSP00000328531.4:n.1673-15C=
ENST00000262186.9:c.2693-15C=	ENSP00000262186.5:n.2693-15C=
ENST00000330883.8:c.1673-15C=	ENSP00000328531.4:n.1673-15C=
NM_000238.3:c.2693-15C= , LRG_288t1:c.2693-15C=	NP_000229.1:n.2693-15C=
NM_172057.2:c.1673-15C= , LRG_288t3:c.1673-15C=	NP_742054.1:n.1673-15C=
XM_011516185.1:c.2393-15C=	XP_011514487.1:n.2393-15C=
XM_011516186.1:c.2693-202C=	XP_011514488.1:n.2693-202C=
XM_011516185.2:c.2393-15C=	XP_011514487.1:n.2393-15C=
XM_011516186.3:c.2693-202C=	XP_011514488.1:n.2693-202C=
XM_017012195.1:c.2543-15C=	XP_016867684.1:n.2543-15C=
XM_017012196.1:c.2516-15C=	XP_016867685.1:n.2516-15C=
NM_000238.4:c.2693-15C= MANE Select	NP_000229.1:n.2693-15C=
NM_172057.3:c.1673-15C=	NP_742054.1:n.1673-15C=