Canonical Allele Identifier: CA2430198302
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54495022C= , CM000685.2:g.54495022C= GRCh38
NC_000023.10:g.54521455C= , CM000685.1:g.54521455C= GRCh37
NC_000023.9:g.54538180C= NCBI36
NG_008054.1:g.6145G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.307+104G= MANE Select ENSP00000364277.3:n.307+104G=
ENST00000375135.3:c.307+104G= ENSP00000364277.3:n.307+104G=
NM_004463.2:c.307+104G= NP_004454.2:n.307+104G=
NM_004463.3:c.307+104G= MANE Select NP_004454.2:n.307+104G=