Canonical Allele Identifier: CA374966474

Gene: FPGS

Linked Data

• gnomAD v4: 9-127813496-T-G
• MyVariant Identifiers: chr9:g.130575775T>G (hg19) ; chr9:g.127813496T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813496T>G , CM000671.2:g.127813496T>G	GRCh38
NC_000009.11:g.130575775T>G , CM000671.1:g.130575775T>G	GRCh37
NC_000009.10:g.129615596T>G	NCBI36
NG_009551.1:g.46273A>C , LRG_589:g.46273A>C
NG_023245.1:g.15622T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1656T>G MANE Select	ENSP00000362344.2:p.Ser552Arg
ENST00000373225.7:c.1506T>G	ENSP00000362322.3:p.Ser502Arg
ENST00000373247.6:c.1656T>G	ENSP00000362344.2:p.Ser552Arg
ENST00000393706.6:c.1578T>G	ENSP00000377309.2:p.Ser526Arg
ENST00000460181.5:n.1644T>G
ENST00000467826.5:n.709+173T>G
ENST00000475270.1:n.482T>G
ENST00000630236.2:c.*380T>G	ENSP00000486766.1:n.*380T>G
NM_001018078.2:c.1506T>G	NP_001018088.1:p.Ser502Arg
NM_001288803.1:c.1578T>G	NP_001275732.1:p.Ser526Arg
NM_004957.5:c.1656T>G	NP_004948.4:p.Ser552Arg
NR_110170.1:n.1704T>G
XM_005251864.2:c.1483+173T>G	XP_005251921.1:n.1483+173T>G
XM_011518437.1:c.1506T>G	XP_011516739.1:p.Ser502Arg
XM_011518438.1:c.1506T>G	XP_011516740.1:p.Ser502Arg
XM_011518439.1:c.813T>G	XP_011516741.1:p.Ser271Arg
XR_242581.2:n.1553T>G
XR_242582.2:n.1380+173T>G
XM_005251864.4:c.1483+173T>G	XP_005251921.1:n.1483+173T>G
XM_011518439.2:c.813T>G	XP_011516741.1:p.Ser271Arg
XM_017014565.2:c.1333+173T>G	XP_016870054.1:n.1333+173T>G
XM_017014566.1:c.813T>G	XP_016870055.1:p.Ser271Arg
XR_242581.4:n.1551T>G
XR_242582.4:n.1378+173T>G
NM_004957.6:c.1656T>G MANE Select	NP_004948.4:p.Ser552Arg