Canonical Allele Identifier: CA2430188978
Gene: FGD1 HGNC NCBI

Linked Data

dbSNP Id: rs1922750514

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54466000_54466001del , CM000685.2:g.54466000_54466001del GRCh38
NC_000023.10:g.54492433_54492434del , CM000685.1:g.54492433_54492434del GRCh37
NC_000023.9:g.54509158_54509159del NCBI36
NG_008054.1:g.35166_35167del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.1341-149_1341-148del MANE Select ENSP00000364277.3:n.1341-149_1341-148del
ENST00000375135.3:c.1341-149_1341-148del ENSP00000364277.3:n.1341-149_1341-148del
NM_004463.2:c.1341-149_1341-148del NP_004454.2:n.1341-149_1341-148del
NM_004463.3:c.1341-149_1341-148del MANE Select NP_004454.2:n.1341-149_1341-148del