Canonical Allele Identifier: CA2430198328
Gene: FGD1 HGNC NCBI

Linked Data

dbSNP Id: rs1923497959

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54495077_54495082del , CM000685.2:g.54495077_54495082del GRCh38
NC_000023.10:g.54521510_54521515del , CM000685.1:g.54521510_54521515del GRCh37
NC_000023.9:g.54538235_54538240del NCBI36
NG_008054.1:g.6089_6094del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.307+48_307+53del MANE Select ENSP00000364277.3:n.307+48_307+53del
ENST00000375135.3:c.307+48_307+53del ENSP00000364277.3:n.307+48_307+53del
NM_004463.2:c.307+48_307+53del NP_004454.2:n.307+48_307+53del
NM_004463.3:c.307+48_307+53del MANE Select NP_004454.2:n.307+48_307+53del