Canonical Allele Identifier: CA1504952199

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604768A= , CM000666.2:g.154604768A=	GRCh38
NC_000004.11:g.155525920A= , CM000666.1:g.155525920A=	GRCh37
NC_000004.10:g.155745370A=	NCBI36
NG_008834.1:g.12983T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.*66T= MANE Select	ENSP00000336829.3:n.*66T=
ENST00000336098.7:c.*66T=	ENSP00000336829.3:n.*66T=
ENST00000404648.7:c.1299+129T=	ENSP00000384860.3:n.1299+129T=
ENST00000405164.5:c.1323+129T=	ENSP00000384101.1:n.1323+129T=
ENST00000407946.5:c.*66T=	ENSP00000384552.1:n.*66T=
ENST00000465913.1:n.976T=
ENST00000492082.5:n.1841+129T=
NM_000509.4:c.1299+129T=	NP_000500.2:n.1299+129T=
NM_000509.5:c.1299+129T=	NP_000500.2:n.1299+129T=
NM_021870.2:c.*66T=	NP_068656.2:n.*66T=
NM_021870.3:c.*66T= MANE Select	NP_068656.2:n.*66T=
NM_000509.6:c.1299+129T=	NP_000500.2:n.1299+129T=