Canonical Allele Identifier: CA467474200

Gene: FPGS

Linked Data

• MyVariant Identifiers: chr9:g.130575802T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813523T>A , CM000671.2:g.127813523T>A	GRCh38
NC_000009.11:g.130575802T>A , CM000671.1:g.130575802T>A	GRCh37
NC_000009.10:g.129615623T>A	NCBI36
NG_009551.1:g.46246A>T , LRG_589:g.46246A>T
NG_023245.1:g.15649T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1683T>A MANE Select	ENSP00000362344.2:p.Ala561=
ENST00000373225.7:c.1533T>A	ENSP00000362322.3:p.Ala511=
ENST00000373247.6:c.1683T>A	ENSP00000362344.2:p.Ala561=
ENST00000393706.6:c.1605T>A	ENSP00000377309.2:p.Ala535=
ENST00000460181.5:n.1671T>A
ENST00000467826.5:n.709+200T>A
ENST00000475270.1:n.509T>A
ENST00000630236.2:c.*407T>A	ENSP00000486766.1:n.*407T>A
NM_001018078.2:c.1533T>A	NP_001018088.1:p.Ala511=
NM_001288803.1:c.1605T>A	NP_001275732.1:p.Ala535=
NM_004957.5:c.1683T>A	NP_004948.4:p.Ala561=
NR_110170.1:n.1731T>A
XM_005251864.2:c.1483+200T>A	XP_005251921.1:n.1483+200T>A
XM_011518437.1:c.1533T>A	XP_011516739.1:p.Ala511=
XM_011518438.1:c.1533T>A	XP_011516740.1:p.Ala511=
XM_011518439.1:c.840T>A	XP_011516741.1:p.Ala280=
XR_242581.2:n.1580T>A
XR_242582.2:n.1380+200T>A
XM_005251864.4:c.1483+200T>A	XP_005251921.1:n.1483+200T>A
XM_011518439.2:c.840T>A	XP_011516741.1:p.Ala280=
XM_017014565.2:c.1333+200T>A	XP_016870054.1:n.1333+200T>A
XM_017014566.1:c.840T>A	XP_016870055.1:p.Ala280=
XR_242581.4:n.1578T>A
XR_242582.4:n.1378+200T>A
NM_004957.6:c.1683T>A MANE Select	NP_004948.4:p.Ala561=