Canonical Allele Identifier: CA1504955463

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154612536A= , CM000666.2:g.154612536A=	GRCh38
NC_000004.11:g.155533688A= , CM000666.1:g.155533688A=	GRCh37
NC_000004.10:g.155753138A=	NCBI36
NG_008834.1:g.5215T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.74T= MANE Select	ENSP00000336829.3:p.Val25=
ENST00000336098.7:c.74T=	ENSP00000336829.3:p.Val25=
ENST00000393846.6:c.-231-101T=	ENSP00000377429.2:n.-231-101T=
ENST00000404648.7:c.74T=	ENSP00000384860.3:p.Val25=
ENST00000405164.5:c.74T=	ENSP00000384101.1:p.Val25=
ENST00000407946.5:c.74T=	ENSP00000384552.1:p.Val25=
ENST00000443553.5:c.-197-101T=	ENSP00000407562.1:n.-197-101T=
ENST00000464532.5:n.121T=
ENST00000465336.1:n.121T=
ENST00000473393.5:n.100T=
ENST00000484695.1:n.76T=
ENST00000492082.5:n.124T=
NM_000509.4:c.74T=	NP_000500.2:p.Val25=
NM_000509.5:c.74T=	NP_000500.2:p.Val25=
NM_021870.2:c.74T=	NP_068656.2:p.Val25=
NM_021870.3:c.74T= MANE Select	NP_068656.2:p.Val25=
NM_000509.6:c.74T=	NP_000500.2:p.Val25=