Canonical Allele Identifier: CA2430188936
Gene: FGD1 HGNC NCBI

Linked Data

dbSNP Id: rs1922747706

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54465859del , CM000685.2:g.54465859del GRCh38
NC_000023.10:g.54492292del , CM000685.1:g.54492292del GRCh37
NC_000023.9:g.54509017del NCBI36
NG_008054.1:g.35308del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.1341-7del MANE Select ENSP00000364277.3:n.1341-7del
ENST00000375135.3:c.1341-7del ENSP00000364277.3:n.1341-7del
NM_004463.2:c.1341-7del NP_004454.2:n.1341-7del
NM_004463.3:c.1341-7del MANE Select NP_004454.2:n.1341-7del