Canonical Allele Identifier: CA1752429743

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947615G= , CM000669.2:g.150947615G=	GRCh38
NC_000007.13:g.150644703G= , CM000669.1:g.150644703G=	GRCh37
NC_000007.12:g.150275636G=	NCBI36
NG_008916.1:g.35312C= , LRG_288:g.35312C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3789C=
ENST00000262186.10:c.2956C= MANE Select	ENSP00000262186.5:p.Pro986=
ENST00000330883.9:c.1936C=	ENSP00000328531.4:p.Pro646=
ENST00000262186.9:c.2956C=	ENSP00000262186.5:p.Pro986=
ENST00000330883.8:c.1936C=	ENSP00000328531.4:p.Pro646=
NM_000238.3:c.2956C= , LRG_288t1:c.2956C=	NP_000229.1:p.Pro986=
NM_172057.2:c.1936C= , LRG_288t3:c.1936C=	NP_742054.1:p.Pro646=
XM_011516185.1:c.2656C=	XP_011514487.1:p.Pro886=
XM_011516186.1:c.*36C=	XP_011514488.1:n.*36C=
XM_011516185.2:c.2656C=	XP_011514487.1:p.Pro886=
XM_011516186.3:c.*36C=	XP_011514488.1:n.*36C=
XM_017012195.1:c.2806C=	XP_016867684.1:p.Pro936=
XM_017012196.1:c.2779C=	XP_016867685.1:p.Pro927=
NM_000238.4:c.2956C= MANE Select	NP_000229.1:p.Pro986=
NM_172057.3:c.1936C=	NP_742054.1:p.Pro646=