Canonical Allele Identifier: CA2430188932
Gene: FGD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54465847C= , CM000685.2:g.54465847C= GRCh38
NC_000023.10:g.54492280C= , CM000685.1:g.54492280C= GRCh37
NC_000023.9:g.54509005C= NCBI36
NG_008054.1:g.35320G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.1346G= MANE Select ENSP00000364277.3:p.Arg449=
ENST00000375135.3:c.1346G= ENSP00000364277.3:p.Arg449=
NM_004463.2:c.1346G= NP_004454.2:p.Arg449=
NM_004463.3:c.1346G= MANE Select NP_004454.2:p.Arg449=
Search 100 bp 5'
Search 100 bp 3'