Canonical Allele Identifier: CA358537152

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154610152G>C , CM000666.2:g.154610152G>C	GRCh38
NC_000004.11:g.155531304G>C , CM000666.1:g.155531304G>C	GRCh37
NC_000004.10:g.155750754G>C	NCBI36
NG_008834.1:g.7599C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021870.3:c.447C>G MANE Select	NP_068656.2:p.Asn149Lys
ENST00000336098.8:c.447C>G MANE Select	ENSP00000336829.3:p.Asn149Lys
NM_000509.4:c.447C>G	NP_000500.2:p.Asn149Lys
NM_000509.5:c.447C>G	NP_000500.2:p.Asn149Lys
NM_000509.6:c.447C>G	NP_000500.2:p.Asn149Lys
NM_021870.2:c.447C>G	NP_068656.2:p.Asn149Lys
ENST00000336098.7:c.447C>G	ENSP00000336829.3:p.Asn149Lys
ENST00000393846.6:c.138C>G	ENSP00000377429.2:p.Asn46Lys
ENST00000404648.7:c.447C>G	ENSP00000384860.3:p.Asn149Lys
ENST00000405164.5:c.447C>G	ENSP00000384101.1:p.Asn149Lys
ENST00000407946.5:c.447C>G	ENSP00000384552.1:p.Asn149Lys
ENST00000443553.5:c.138C>G	ENSP00000407562.1:p.Asn46Lys
ENST00000464532.5:n.494C>G
ENST00000492082.5:n.686C>G