Canonical Allele Identifier: CA2430188949
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54465905A= , CM000685.2:g.54465905A= GRCh38
NC_000023.10:g.54492338A= , CM000685.1:g.54492338A= GRCh37
NC_000023.9:g.54509063A= NCBI36
NG_008054.1:g.35262T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.1341-53T= MANE Select ENSP00000364277.3:n.1341-53T=
ENST00000375135.3:c.1341-53T= ENSP00000364277.3:n.1341-53T=
NM_004463.2:c.1341-53T= NP_004454.2:n.1341-53T=
NM_004463.3:c.1341-53T= MANE Select NP_004454.2:n.1341-53T=