Canonical Allele Identifier: CA1879977079

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813408C= , CM000671.2:g.127813408C=	GRCh38
NC_000009.11:g.130575687C= , CM000671.1:g.130575687C=	GRCh37
NC_000009.10:g.129615508C=	NCBI36
NG_009551.1:g.46361G= , LRG_589:g.46361G=
NG_023245.1:g.15534C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1568C= MANE Select	ENSP00000362344.2:p.Ala523=
ENST00000373225.7:c.1418C=	ENSP00000362322.3:p.Ala473=
ENST00000373228.5:c.*225C=	ENSP00000362325.1:n.*225C=
ENST00000373247.6:c.1568C=	ENSP00000362344.2:p.Ala523=
ENST00000393706.6:c.1490C=	ENSP00000377309.2:p.Ala497=
ENST00000460181.5:n.1556C=
ENST00000467826.5:n.709+85C=
ENST00000475270.1:n.394C=
ENST00000630236.2:c.*292C=	ENSP00000486766.1:n.*292C=
NM_001018078.2:c.1418C=	NP_001018088.1:p.Ala473=
NM_001288803.1:c.1490C=	NP_001275732.1:p.Ala497=
NM_004957.5:c.1568C=	NP_004948.4:p.Ala523=
NR_110170.1:n.1616C=
XM_005251864.2:c.1483+85C=	XP_005251921.1:n.1483+85C=
XM_011518437.1:c.1418C=	XP_011516739.1:p.Ala473=
XM_011518438.1:c.1418C=	XP_011516740.1:p.Ala473=
XM_011518439.1:c.725C=	XP_011516741.1:p.Ala242=
XR_242581.2:n.1465C=
XR_242582.2:n.1380+85C=
XM_005251864.4:c.1483+85C=	XP_005251921.1:n.1483+85C=
XM_011518439.2:c.725C=	XP_011516741.1:p.Ala242=
XM_017014565.2:c.1333+85C=	XP_016870054.1:n.1333+85C=
XM_017014566.1:c.725C=	XP_016870055.1:p.Ala242=
XR_242581.4:n.1463C=
XR_242582.4:n.1378+85C=
NM_004957.6:c.1568C= MANE Select	NP_004948.4:p.Ala523=