Canonical Allele Identifier: CA374965760

Gene: FPGS

Linked Data

• dbSNP Id: rs1363025842
• gnomAD v2: 9-130575716-C-A
• gnomAD v4: 9-127813437-C-A
• MyVariant Identifiers: chr9:g.130575716C>A (hg19) ; chr9:g.127813437C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813437C>A , CM000671.2:g.127813437C>A	GRCh38
NC_000009.11:g.130575716C>A , CM000671.1:g.130575716C>A	GRCh37
NC_000009.10:g.129615537C>A	NCBI36
NG_009551.1:g.46332G>T , LRG_589:g.46332G>T
NG_023245.1:g.15563C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1597C>A MANE Select	ENSP00000362344.2:p.Pro533Thr
ENST00000373225.7:c.1447C>A	ENSP00000362322.3:p.Pro483Thr
ENST00000373247.6:c.1597C>A	ENSP00000362344.2:p.Pro533Thr
ENST00000393706.6:c.1519C>A	ENSP00000377309.2:p.Pro507Thr
ENST00000460181.5:n.1585C>A
ENST00000467826.5:n.709+114C>A
ENST00000475270.1:n.423C>A
ENST00000630236.2:c.*321C>A	ENSP00000486766.1:n.*321C>A
NM_001018078.2:c.1447C>A	NP_001018088.1:p.Pro483Thr
NM_001288803.1:c.1519C>A	NP_001275732.1:p.Pro507Thr
NM_004957.5:c.1597C>A	NP_004948.4:p.Pro533Thr
NR_110170.1:n.1645C>A
XM_005251864.2:c.1483+114C>A	XP_005251921.1:n.1483+114C>A
XM_011518437.1:c.1447C>A	XP_011516739.1:p.Pro483Thr
XM_011518438.1:c.1447C>A	XP_011516740.1:p.Pro483Thr
XM_011518439.1:c.754C>A	XP_011516741.1:p.Pro252Thr
XR_242581.2:n.1494C>A
XR_242582.2:n.1380+114C>A
XM_005251864.4:c.1483+114C>A	XP_005251921.1:n.1483+114C>A
XM_011518439.2:c.754C>A	XP_011516741.1:p.Pro252Thr
XM_017014565.2:c.1333+114C>A	XP_016870054.1:n.1333+114C>A
XM_017014566.1:c.754C>A	XP_016870055.1:p.Pro252Thr
XR_242581.4:n.1492C>A
XR_242582.4:n.1378+114C>A
NM_004957.6:c.1597C>A MANE Select	NP_004948.4:p.Pro533Thr