Canonical Allele Identifier: CA358535100

Gene: FGG

Linked Data

• MyVariant Identifiers: chr4:g.155526035T>C (hg19) ; chr4:g.154604883T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604883T>C , CM000666.2:g.154604883T>C	GRCh38
NC_000004.11:g.155526035T>C , CM000666.1:g.155526035T>C	GRCh37
NC_000004.10:g.155745485T>C	NCBI36
NG_008834.1:g.12868A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1313A>G MANE Select	ENSP00000336829.3:p.His438Arg
ENST00000336098.7:c.1313A>G	ENSP00000336829.3:p.His438Arg
ENST00000404648.7:c.1299+14A>G	ENSP00000384860.3:n.1299+14A>G
ENST00000405164.5:c.1323+14A>G	ENSP00000384101.1:n.1323+14A>G
ENST00000407946.5:c.1337A>G	ENSP00000384552.1:p.His446Arg
ENST00000465913.1:n.861A>G
ENST00000492082.5:n.1841+14A>G
NM_000509.4:c.1299+14A>G	NP_000500.2:n.1299+14A>G
NM_000509.5:c.1299+14A>G	NP_000500.2:n.1299+14A>G
NM_021870.2:c.1313A>G	NP_068656.2:p.His438Arg
NM_021870.3:c.1313A>G MANE Select	NP_068656.2:p.His438Arg
NM_000509.6:c.1299+14A>G	NP_000500.2:n.1299+14A>G