Canonical Allele Identifier: CA2499226799
Community Standard Title: NM_004463.3(FGD1):c.367del (p.Leu123Ter)
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54471429del , CM000685.2:g.54471429del GRCh38
NC_000023.10:g.54497862del , CM000685.1:g.54497862del GRCh37
NC_000023.9:g.54514587del NCBI36
NG_008054.1:g.29739del

Transcript Alleles

HGVS Amino-acid Change
NM_004463.3:c.367del MANE Select NP_004454.2:p.Leu123Ter
ENST00000375135.4:c.367del MANE Select ENSP00000364277.3:p.Leu123Ter
NM_004463.2:c.367del NP_004454.2:p.Leu123Ter
ENST00000375135.3:c.367del ENSP00000364277.3:p.Leu123Ter