Canonical Allele Identifier: CA358535468
Gene: FGG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154605051T>G , CM000666.2:g.154605051T>G GRCh38
NC_000004.11:g.155526203T>G , CM000666.1:g.155526203T>G GRCh37
NC_000004.10:g.155745653T>G NCBI36
NG_008834.1:g.12700A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336098.8:c.1145A>C MANE Select ENSP00000336829.3:p.Lys382Thr
ENST00000336098.7:c.1145A>C ENSP00000336829.3:p.Lys382Thr
ENST00000404648.7:c.1145A>C ENSP00000384860.3:p.Lys382Thr
ENST00000405164.5:c.1169A>C ENSP00000384101.1:p.Lys390Thr
ENST00000407946.5:c.1169A>C ENSP00000384552.1:p.Lys390Thr
ENST00000465913.1:n.693A>C
ENST00000492082.5:n.1687A>C
NM_000509.4:c.1145A>C NP_000500.2:p.Lys382Thr
NM_000509.5:c.1145A>C NP_000500.2:p.Lys382Thr
NM_021870.2:c.1145A>C NP_068656.2:p.Lys382Thr
NM_021870.3:c.1145A>C MANE Select NP_068656.2:p.Lys382Thr
NM_000509.6:c.1145A>C NP_000500.2:p.Lys382Thr