Canonical Allele Identifier: CA2430198335
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54495085C= , CM000685.2:g.54495085C= GRCh38
NC_000023.10:g.54521518C= , CM000685.1:g.54521518C= GRCh37
NC_000023.9:g.54538243C= NCBI36
NG_008054.1:g.6082G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.307+41G= MANE Select ENSP00000364277.3:n.307+41G=
ENST00000375135.3:c.307+41G= ENSP00000364277.3:n.307+41G=
NM_004463.2:c.307+41G= NP_004454.2:n.307+41G=
NM_004463.3:c.307+41G= MANE Select NP_004454.2:n.307+41G=