Canonical Allele Identifier: CA1752432101

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150949043T= , CM000669.2:g.150949043T=	GRCh38
NC_000007.13:g.150646131T= , CM000669.1:g.150646131T=	GRCh37
NC_000007.12:g.150277064T=	NCBI36
NG_008916.1:g.33884A= , LRG_288:g.33884A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3238A=
ENST00000262186.10:c.2405A= MANE Select	ENSP00000262186.5:p.Asn802=
ENST00000330883.9:c.1385A=	ENSP00000328531.4:p.Asn462=
ENST00000262186.9:c.2405A=	ENSP00000262186.5:p.Asn802=
ENST00000330883.8:c.1385A=	ENSP00000328531.4:p.Asn462=
NM_000238.3:c.2405A= , LRG_288t1:c.2405A=	NP_000229.1:p.Asn802=
NM_172057.2:c.1385A= , LRG_288t3:c.1385A=	NP_742054.1:p.Asn462=
XM_011516185.1:c.2105A=	XP_011514487.1:p.Asn702=
XM_011516186.1:c.2405A=	XP_011514488.1:p.Asn802=
XM_011516185.2:c.2105A=	XP_011514487.1:p.Asn702=
XM_011516186.3:c.2405A=	XP_011514488.1:p.Asn802=
XM_017012195.1:c.2255A=	XP_016867684.1:p.Asn752=
XM_017012196.1:c.2228A=	XP_016867685.1:p.Asn743=
NM_000238.4:c.2405A= MANE Select	NP_000229.1:p.Asn802=
NM_172057.3:c.1385A=	NP_742054.1:p.Asn462=