Canonical Allele Identifier: CA1504955220

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154612013C= , CM000666.2:g.154612013C=	GRCh38
NC_000004.11:g.155533165C= , CM000666.1:g.155533165C=	GRCh37
NC_000004.10:g.155752615C=	NCBI36
NG_008834.1:g.5738G=

Transcript Alleles

HGVS	Amino-acid Change
NM_021870.3:c.307+5G= MANE Select	NP_068656.2:n.307+5G=
ENST00000336098.8:c.307+5G= MANE Select	ENSP00000336829.3:n.307+5G=
NM_000509.4:c.307+5G=	NP_000500.2:n.307+5G=
NM_000509.5:c.307+5G=	NP_000500.2:n.307+5G=
NM_000509.6:c.307+5G=	NP_000500.2:n.307+5G=
NM_021870.2:c.307+5G=	NP_068656.2:n.307+5G=
ENST00000336098.7:c.307+5G=	ENSP00000336829.3:n.307+5G=
ENST00000393846.6:c.-3+5G=	ENSP00000377429.2:n.-3+5G=
ENST00000404648.7:c.307+5G=	ENSP00000384860.3:n.307+5G=
ENST00000405164.5:c.307+5G=	ENSP00000384101.1:n.307+5G=
ENST00000407946.5:c.307+5G=	ENSP00000384552.1:n.307+5G=
ENST00000443553.5:c.-3+5G=	ENSP00000407562.1:n.-3+5G=
ENST00000464532.5:n.354+5G=
ENST00000465336.1:n.548G=
ENST00000473393.5:n.333+5G=
ENST00000484695.1:n.314G=
ENST00000492082.5:n.546+5G=