Canonical Allele Identifier: CA358535189

Gene: FGG

Linked Data

• gnomAD v4: 4-154604925-T-C
• MyVariant Identifiers: chr4:g.155526077T>C (hg19) ; chr4:g.154604925T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604925T>C , CM000666.2:g.154604925T>C	GRCh38
NC_000004.11:g.155526077T>C , CM000666.1:g.155526077T>C	GRCh37
NC_000004.10:g.155745527T>C	NCBI36
NG_008834.1:g.12826A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1271A>G MANE Select	ENSP00000336829.3:p.Gln424Arg
ENST00000336098.7:c.1271A>G	ENSP00000336829.3:p.Gln424Arg
ENST00000404648.7:c.1271A>G	ENSP00000384860.3:p.Gln424Arg
ENST00000405164.5:c.1295A>G	ENSP00000384101.1:p.Gln432Arg
ENST00000407946.5:c.1295A>G	ENSP00000384552.1:p.Gln432Arg
ENST00000465913.1:n.819A>G
ENST00000492082.5:n.1813A>G
NM_000509.4:c.1271A>G	NP_000500.2:p.Gln424Arg
NM_000509.5:c.1271A>G	NP_000500.2:p.Gln424Arg
NM_021870.2:c.1271A>G	NP_068656.2:p.Gln424Arg
NM_021870.3:c.1271A>G MANE Select	NP_068656.2:p.Gln424Arg
NM_000509.6:c.1271A>G	NP_000500.2:p.Gln424Arg