Canonical Allele Identifier: CA413244280
Gene: FGD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.54492128C>T (hg19) chrX:g.54465695C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.54465695C>T , CM000685.2:g.54465695C>T GRCh38
NC_000023.10:g.54492128C>T , CM000685.1:g.54492128C>T GRCh37
NC_000023.9:g.54508853C>T NCBI36
NG_008054.1:g.35472G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375135.4:c.1497+1G>A MANE Select ENSP00000364277.3:n.1497+1G>A
ENST00000375135.3:c.1497+1G>A ENSP00000364277.3:n.1497+1G>A
NM_004463.2:c.1497+1G>A NP_004454.2:n.1497+1G>A
NM_004463.3:c.1497+1G>A MANE Select NP_004454.2:n.1497+1G>A
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