Canonical Allele Identifier: CA1504952289

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154605007T= , CM000666.2:g.154605007T=	GRCh38
NC_000004.11:g.155526159T= , CM000666.1:g.155526159T=	GRCh37
NC_000004.10:g.155745609T=	NCBI36
NG_008834.1:g.12744A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1189A= MANE Select	ENSP00000336829.3:p.Thr397=
ENST00000336098.7:c.1189A=	ENSP00000336829.3:p.Thr397=
ENST00000404648.7:c.1189A=	ENSP00000384860.3:p.Thr397=
ENST00000405164.5:c.1213A=	ENSP00000384101.1:p.Thr405=
ENST00000407946.5:c.1213A=	ENSP00000384552.1:p.Thr405=
ENST00000465913.1:n.737A=
ENST00000492082.5:n.1731A=
NM_000509.4:c.1189A=	NP_000500.2:p.Thr397=
NM_000509.5:c.1189A=	NP_000500.2:p.Thr397=
NM_021870.2:c.1189A=	NP_068656.2:p.Thr397=
NM_021870.3:c.1189A= MANE Select	NP_068656.2:p.Thr397=
NM_000509.6:c.1189A=	NP_000500.2:p.Thr397=