Canonical Allele Identifier: CA358536607

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154609635G>T , CM000666.2:g.154609635G>T	GRCh38
NC_000004.11:g.155530787G>T , CM000666.1:g.155530787G>T	GRCh37
NC_000004.10:g.155750237G>T	NCBI36
NG_008834.1:g.8116C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021870.3:c.661C>A MANE Select	NP_068656.2:p.Gln221Lys
ENST00000336098.8:c.661C>A MANE Select	ENSP00000336829.3:p.Gln221Lys
NM_000509.4:c.661C>A	NP_000500.2:p.Gln221Lys
NM_000509.5:c.661C>A	NP_000500.2:p.Gln221Lys
NM_000509.6:c.661C>A	NP_000500.2:p.Gln221Lys
NM_021870.2:c.661C>A	NP_068656.2:p.Gln221Lys
ENST00000336098.7:c.661C>A	ENSP00000336829.3:p.Gln221Lys
ENST00000393846.6:c.352C>A	ENSP00000377429.2:p.Gln118Lys
ENST00000404648.7:c.661C>A	ENSP00000384860.3:p.Gln221Lys
ENST00000405164.5:c.685C>A	ENSP00000384101.1:p.Gln229Lys
ENST00000407946.5:c.685C>A	ENSP00000384552.1:p.Gln229Lys
ENST00000443553.5:c.352C>A	ENSP00000407562.1:p.Gln118Lys
ENST00000465913.1:n.209C>A
ENST00000492082.5:n.1203C>A