Canonical Allele Identifier: CA2430198351
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54495140G= , CM000685.2:g.54495140G= GRCh38
NC_000023.10:g.54521573G= , CM000685.1:g.54521573G= GRCh37
NC_000023.9:g.54538298G= NCBI36
NG_008054.1:g.6027C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.293C= MANE Select ENSP00000364277.3:p.Ser98=
ENST00000375135.3:c.293C= ENSP00000364277.3:p.Ser98=
NM_004463.2:c.293C= NP_004454.2:p.Ser98=
NM_004463.3:c.293C= MANE Select NP_004454.2:p.Ser98=