Canonical Allele Identifier: CA374965599

Gene: FPGS

Linked Data

• gnomAD v4: 9-127813420-T-A
• MyVariant Identifiers: chr9:g.130575699T>A (hg19) ; chr9:g.127813420T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813420T>A , CM000671.2:g.127813420T>A	GRCh38
NC_000009.11:g.130575699T>A , CM000671.1:g.130575699T>A	GRCh37
NC_000009.10:g.129615520T>A	NCBI36
NG_009551.1:g.46349A>T , LRG_589:g.46349A>T
NG_023245.1:g.15546T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1580T>A MANE Select	ENSP00000362344.2:p.Ile527Asn
ENST00000373225.7:c.1430T>A	ENSP00000362322.3:p.Ile477Asn
ENST00000373228.5:c.*237T>A	ENSP00000362325.1:n.*237T>A
ENST00000373247.6:c.1580T>A	ENSP00000362344.2:p.Ile527Asn
ENST00000393706.6:c.1502T>A	ENSP00000377309.2:p.Ile501Asn
ENST00000460181.5:n.1568T>A
ENST00000467826.5:n.709+97T>A
ENST00000475270.1:n.406T>A
ENST00000630236.2:c.*304T>A	ENSP00000486766.1:n.*304T>A
NM_001018078.2:c.1430T>A	NP_001018088.1:p.Ile477Asn
NM_001288803.1:c.1502T>A	NP_001275732.1:p.Ile501Asn
NM_004957.5:c.1580T>A	NP_004948.4:p.Ile527Asn
NR_110170.1:n.1628T>A
XM_005251864.2:c.1483+97T>A	XP_005251921.1:n.1483+97T>A
XM_011518437.1:c.1430T>A	XP_011516739.1:p.Ile477Asn
XM_011518438.1:c.1430T>A	XP_011516740.1:p.Ile477Asn
XM_011518439.1:c.737T>A	XP_011516741.1:p.Ile246Asn
XR_242581.2:n.1477T>A
XR_242582.2:n.1380+97T>A
XM_005251864.4:c.1483+97T>A	XP_005251921.1:n.1483+97T>A
XM_011518439.2:c.737T>A	XP_011516741.1:p.Ile246Asn
XM_017014565.2:c.1333+97T>A	XP_016870054.1:n.1333+97T>A
XM_017014566.1:c.737T>A	XP_016870055.1:p.Ile246Asn
XR_242581.4:n.1475T>A
XR_242582.4:n.1378+97T>A
NM_004957.6:c.1580T>A MANE Select	NP_004948.4:p.Ile527Asn