Canonical Allele Identifier: CA1504952151
Gene: FGG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154604652T= , CM000666.2:g.154604652T= GRCh38
NC_000004.11:g.155525804T= , CM000666.1:g.155525804T= GRCh37
NC_000004.10:g.155745254T= NCBI36
NG_008834.1:g.13099A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336098.8:c.*182A= MANE Select ENSP00000336829.3:n.*182A=
ENST00000336098.7:c.*182A= ENSP00000336829.3:n.*182A=
ENST00000404648.7:c.1299+245A= ENSP00000384860.3:n.1299+245A=
ENST00000405164.5:c.1323+245A= ENSP00000384101.1:n.1323+245A=
ENST00000407946.5:c.*182A= ENSP00000384552.1:n.*182A=
ENST00000465913.1:n.1092A=
ENST00000492082.5:n.1841+245A=
NM_000509.4:c.1299+245A= NP_000500.2:n.1299+245A=
NM_000509.5:c.1299+245A= NP_000500.2:n.1299+245A=
NM_021870.2:c.*182A= NP_068656.2:n.*182A=
NM_021870.3:c.*182A= MANE Select NP_068656.2:n.*182A=
NM_000509.6:c.1299+245A= NP_000500.2:n.1299+245A=