Canonical Allele Identifier: CA1504953960

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154608970T= , CM000666.2:g.154608970T=	GRCh38
NC_000004.11:g.155530122T= , CM000666.1:g.155530122T=	GRCh37
NC_000004.10:g.155749572T=	NCBI36
NG_008834.1:g.8781A=

Transcript Alleles

HGVS	Amino-acid Change
NM_021870.3:c.667-320A= MANE Select	NP_068656.2:n.667-320A=
ENST00000336098.8:c.667-320A= MANE Select	ENSP00000336829.3:n.667-320A=
NM_000509.4:c.667-320A=	NP_000500.2:n.667-320A=
NM_000509.5:c.667-320A=	NP_000500.2:n.667-320A=
NM_000509.6:c.667-320A=	NP_000500.2:n.667-320A=
NM_021870.2:c.667-320A=	NP_068656.2:n.667-320A=
ENST00000336098.7:c.667-320A=	ENSP00000336829.3:n.667-320A=
ENST00000404648.7:c.667-320A=	ENSP00000384860.3:n.667-320A=
ENST00000405164.5:c.691-320A=	ENSP00000384101.1:n.691-320A=
ENST00000407946.5:c.691-320A=	ENSP00000384552.1:n.691-320A=
ENST00000443553.5:c.358-320A=	ENSP00000407562.1:n.358-320A=
ENST00000465913.1:n.215-320A=
ENST00000492082.5:n.1209-320A=