Canonical Allele Identifier: CA2430198307
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54495028T= , CM000685.2:g.54495028T= GRCh38
NC_000023.10:g.54521461T= , CM000685.1:g.54521461T= GRCh37
NC_000023.9:g.54538186T= NCBI36
NG_008054.1:g.6139A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.307+98A= MANE Select ENSP00000364277.3:n.307+98A=
ENST00000375135.3:c.307+98A= ENSP00000364277.3:n.307+98A=
NM_004463.2:c.307+98A= NP_004454.2:n.307+98A=
NM_004463.3:c.307+98A= MANE Select NP_004454.2:n.307+98A=