Canonical Allele Identifier: CA2430188959
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54465932G= , CM000685.2:g.54465932G= GRCh38
NC_000023.10:g.54492365G= , CM000685.1:g.54492365G= GRCh37
NC_000023.9:g.54509090G= NCBI36
NG_008054.1:g.35235C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.1341-80C= MANE Select ENSP00000364277.3:n.1341-80C=
ENST00000375135.3:c.1341-80C= ENSP00000364277.3:n.1341-80C=
NM_004463.2:c.1341-80C= NP_004454.2:n.1341-80C=
NM_004463.3:c.1341-80C= MANE Select NP_004454.2:n.1341-80C=