Canonical Allele Identifier: CA516574645
Gene: FGD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.54521575G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54495142G>C , CM000685.2:g.54495142G>C GRCh38
NC_000023.10:g.54521575G>C , CM000685.1:g.54521575G>C GRCh37
NC_000023.9:g.54538300G>C NCBI36
NG_008054.1:g.6025C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.291C>G MANE Select ENSP00000364277.3:p.Gly97=
ENST00000375135.3:c.291C>G ENSP00000364277.3:p.Gly97=
NM_004463.2:c.291C>G NP_004454.2:p.Gly97=
NM_004463.3:c.291C>G MANE Select NP_004454.2:p.Gly97=