Canonical Allele Identifier: CA358538564

Gene: FGG

Linked Data

• MyVariant Identifiers: chr4:g.155533580G>C (hg19) ; chr4:g.154612428G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154612428G>C , CM000666.2:g.154612428G>C	GRCh38
NC_000004.11:g.155533580G>C , CM000666.1:g.155533580G>C	GRCh37
NC_000004.10:g.155753030G>C	NCBI36
NG_008834.1:g.5323C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.86C>G MANE Select	ENSP00000336829.3:p.Ala29Gly
ENST00000336098.7:c.86C>G	ENSP00000336829.3:p.Ala29Gly
ENST00000393846.6:c.-224C>G	ENSP00000377429.2:n.-224C>G
ENST00000404648.7:c.86C>G	ENSP00000384860.3:p.Ala29Gly
ENST00000405164.5:c.86C>G	ENSP00000384101.1:p.Ala29Gly
ENST00000407946.5:c.86C>G	ENSP00000384552.1:p.Ala29Gly
ENST00000443553.5:c.-190C>G	ENSP00000407562.1:n.-190C>G
ENST00000464532.5:n.133C>G
ENST00000465336.1:n.133C>G
ENST00000473393.5:n.112C>G
ENST00000484695.1:n.88C>G
ENST00000492082.5:n.136C>G
NM_000509.4:c.86C>G	NP_000500.2:p.Ala29Gly
NM_000509.5:c.86C>G	NP_000500.2:p.Ala29Gly
NM_021870.2:c.86C>G	NP_068656.2:p.Ala29Gly
NM_021870.3:c.86C>G MANE Select	NP_068656.2:p.Ala29Gly
NM_000509.6:c.86C>G	NP_000500.2:p.Ala29Gly