Canonical Allele Identifier: CA1879976872

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813334A= , CM000671.2:g.127813334A=	GRCh38
NC_000009.11:g.130575613A= , CM000671.1:g.130575613A=	GRCh37
NC_000009.10:g.129615434A=	NCBI36
NG_009551.1:g.46435T= , LRG_589:g.46435T=
NG_023245.1:g.15460A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1494A= MANE Select	ENSP00000362344.2:p.Ala498=
ENST00000373225.7:c.1344A=	ENSP00000362322.3:p.Ala448=
ENST00000373228.5:c.*151A=	ENSP00000362325.1:n.*151A=
ENST00000373247.6:c.1494A=	ENSP00000362344.2:p.Ala498=
ENST00000393706.6:c.1416A=	ENSP00000377309.2:p.Ala472=
ENST00000460181.5:n.1482A=
ENST00000467826.5:n.709+11A=
ENST00000475270.1:n.320A=
ENST00000630236.2:c.*218A=	ENSP00000486766.1:n.*218A=
NM_001018078.2:c.1344A=	NP_001018088.1:p.Ala448=
NM_001288803.1:c.1416A=	NP_001275732.1:p.Ala472=
NM_004957.5:c.1494A=	NP_004948.4:p.Ala498=
NR_110170.1:n.1542A=
XM_005251864.2:c.1483+11A=	XP_005251921.1:n.1483+11A=
XM_011518437.1:c.1344A=	XP_011516739.1:p.Ala448=
XM_011518438.1:c.1344A=	XP_011516740.1:p.Ala448=
XM_011518439.1:c.651A=	XP_011516741.1:p.Ala217=
XR_242581.2:n.1391A=
XR_242582.2:n.1380+11A=
XM_005251864.4:c.1483+11A=	XP_005251921.1:n.1483+11A=
XM_011518439.2:c.651A=	XP_011516741.1:p.Ala217=
XM_017014565.2:c.1333+11A=	XP_016870054.1:n.1333+11A=
XM_017014566.1:c.651A=	XP_016870055.1:p.Ala217=
XR_242581.4:n.1389A=
XR_242582.4:n.1378+11A=
NM_004957.6:c.1494A= MANE Select	NP_004948.4:p.Ala498=