Canonical Allele Identifier: CA413254399

Gene: FGD1

Linked Data

• MyVariant Identifiers: chrX:g.54521569C>G (hg19) ; chrX:g.54495136C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54495136C>G , CM000685.2:g.54495136C>G	GRCh38
NC_000023.10:g.54521569C>G , CM000685.1:g.54521569C>G	GRCh37
NC_000023.9:g.54538294C>G	NCBI36
NG_008054.1:g.6031G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375135.4:c.297G>C MANE Select	ENSP00000364277.3:p.Gln99His
ENST00000375135.3:c.297G>C	ENSP00000364277.3:p.Gln99His
NM_004463.2:c.297G>C	NP_004454.2:p.Gln99His
NM_004463.3:c.297G>C MANE Select	NP_004454.2:p.Gln99His