Canonical Allele Identifier: CA413245211
Gene: FGD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54465832C>G , CM000685.2:g.54465832C>G GRCh38
NC_000023.10:g.54492265C>G , CM000685.1:g.54492265C>G GRCh37
NC_000023.9:g.54508990C>G NCBI36
NG_008054.1:g.35335G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.1361G>C MANE Select ENSP00000364277.3:p.Gly454Ala
ENST00000375135.3:c.1361G>C ENSP00000364277.3:p.Gly454Ala
NM_004463.2:c.1361G>C NP_004454.2:p.Gly454Ala
NM_004463.3:c.1361G>C MANE Select NP_004454.2:p.Gly454Ala