Canonical Allele Identifier: CA2430198296
Gene: FGD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54495011G= , CM000685.2:g.54495011G= GRCh38
NC_000023.10:g.54521444G= , CM000685.1:g.54521444G= GRCh37
NC_000023.9:g.54538169G= NCBI36
NG_008054.1:g.6156C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.307+115C= MANE Select ENSP00000364277.3:n.307+115C=
ENST00000375135.3:c.307+115C= ENSP00000364277.3:n.307+115C=
NM_004463.2:c.307+115C= NP_004454.2:n.307+115C=
NM_004463.3:c.307+115C= MANE Select NP_004454.2:n.307+115C=