Canonical Allele Identifier: CA2430198332
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54495078A= , CM000685.2:g.54495078A= GRCh38
NC_000023.10:g.54521511A= , CM000685.1:g.54521511A= GRCh37
NC_000023.9:g.54538236A= NCBI36
NG_008054.1:g.6089T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.307+48T= MANE Select ENSP00000364277.3:n.307+48T=
ENST00000375135.3:c.307+48T= ENSP00000364277.3:n.307+48T=
NM_004463.2:c.307+48T= NP_004454.2:n.307+48T=
NM_004463.3:c.307+48T= MANE Select NP_004454.2:n.307+48T=