Canonical Allele Identifier: CA374967369

Gene: FPGS

Linked Data

• gnomAD v4: 9-127813581-C-A
• MyVariant Identifiers: chr9:g.130575860C>A (hg19) ; chr9:g.127813581C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813581C>A , CM000671.2:g.127813581C>A	GRCh38
NC_000009.11:g.130575860C>A , CM000671.1:g.130575860C>A	GRCh37
NC_000009.10:g.129615681C>A	NCBI36
NG_009551.1:g.46188G>T , LRG_589:g.46188G>T
NG_023245.1:g.15707C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1741C>A MANE Select	ENSP00000362344.2:p.Leu581Met
ENST00000373225.7:c.1591C>A	ENSP00000362322.3:p.Leu531Met
ENST00000373247.6:c.1741C>A	ENSP00000362344.2:p.Leu581Met
ENST00000393706.6:c.1663C>A	ENSP00000377309.2:p.Leu555Met
ENST00000460181.5:n.1729C>A
ENST00000467826.5:n.709+258C>A
ENST00000630236.2:c.*465C>A	ENSP00000486766.1:n.*465C>A
NM_001018078.2:c.1591C>A	NP_001018088.1:p.Leu531Met
NM_001288803.1:c.1663C>A	NP_001275732.1:p.Leu555Met
NM_004957.5:c.1741C>A	NP_004948.4:p.Leu581Met
NR_110170.1:n.1789C>A
XM_005251864.2:c.1483+258C>A	XP_005251921.1:n.1483+258C>A
XM_011518437.1:c.1591C>A	XP_011516739.1:p.Leu531Met
XM_011518438.1:c.1591C>A	XP_011516740.1:p.Leu531Met
XM_011518439.1:c.898C>A	XP_011516741.1:p.Leu300Met
XR_242581.2:n.1638C>A
XR_242582.2:n.1380+258C>A
XM_005251864.4:c.1483+258C>A	XP_005251921.1:n.1483+258C>A
XM_011518439.2:c.898C>A	XP_011516741.1:p.Leu300Met
XM_017014565.2:c.1333+258C>A	XP_016870054.1:n.1333+258C>A
XM_017014566.1:c.898C>A	XP_016870055.1:p.Leu300Met
XR_242581.4:n.1636C>A
XR_242582.4:n.1378+258C>A
NM_004957.6:c.1741C>A MANE Select	NP_004948.4:p.Leu581Met