Canonical Allele Identifier: CA1504955408

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154612434T= , CM000666.2:g.154612434T=	GRCh38
NC_000004.11:g.155533586T= , CM000666.1:g.155533586T=	GRCh37
NC_000004.10:g.155753036T=	NCBI36
NG_008834.1:g.5317A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.80A= MANE Select	ENSP00000336829.3:p.Tyr27=
ENST00000336098.7:c.80A=	ENSP00000336829.3:p.Tyr27=
ENST00000393846.6:c.-230A=	ENSP00000377429.2:n.-230A=
ENST00000404648.7:c.80A=	ENSP00000384860.3:p.Tyr27=
ENST00000405164.5:c.80A=	ENSP00000384101.1:p.Tyr27=
ENST00000407946.5:c.80A=	ENSP00000384552.1:p.Tyr27=
ENST00000443553.5:c.-196A=	ENSP00000407562.1:n.-196A=
ENST00000464532.5:n.127A=
ENST00000465336.1:n.127A=
ENST00000473393.5:n.106A=
ENST00000484695.1:n.82A=
ENST00000492082.5:n.130A=
NM_000509.4:c.80A=	NP_000500.2:p.Tyr27=
NM_000509.5:c.80A=	NP_000500.2:p.Tyr27=
NM_021870.2:c.80A=	NP_068656.2:p.Tyr27=
NM_021870.3:c.80A= MANE Select	NP_068656.2:p.Tyr27=
NM_000509.6:c.80A=	NP_000500.2:p.Tyr27=