Canonical Allele Identifier: CA1504953079

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154606932C= , CM000666.2:g.154606932C=	GRCh38
NC_000004.11:g.155528084C= , CM000666.1:g.155528084C=	GRCh37
NC_000004.10:g.155747534C=	NCBI36
NG_008834.1:g.10819G=

Transcript Alleles

HGVS	Amino-acid Change
NM_021870.3:c.902G= MANE Select	NP_068656.2:p.Arg301=
ENST00000336098.8:c.902G= MANE Select	ENSP00000336829.3:p.Arg301=
NM_000509.4:c.902G=	NP_000500.2:p.Arg301=
NM_000509.5:c.902G=	NP_000500.2:p.Arg301=
NM_000509.6:c.902G=	NP_000500.2:p.Arg301=
NM_021870.2:c.902G=	NP_068656.2:p.Arg301=
ENST00000336098.7:c.902G=	ENSP00000336829.3:p.Arg301=
ENST00000404648.7:c.902G=	ENSP00000384860.3:p.Arg301=
ENST00000405164.5:c.926G=	ENSP00000384101.1:p.Arg309=
ENST00000407946.5:c.926G=	ENSP00000384552.1:p.Arg309=
ENST00000465913.1:n.450G=
ENST00000492082.5:n.1444G=