Canonical Allele Identifier: CA1879977407

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813593C= , CM000671.2:g.127813593C=	GRCh38
NC_000009.11:g.130575872C= , CM000671.1:g.130575872C=	GRCh37
NC_000009.10:g.129615693C=	NCBI36
NG_009551.1:g.46176G= , LRG_589:g.46176G=
NG_023245.1:g.15719C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1753C= MANE Select	ENSP00000362344.2:p.Leu585=
ENST00000373225.7:c.1603C=	ENSP00000362322.3:p.Leu535=
ENST00000373247.6:c.1753C=	ENSP00000362344.2:p.Leu585=
ENST00000393706.6:c.1675C=	ENSP00000377309.2:p.Leu559=
ENST00000460181.5:n.1741C=
ENST00000467826.5:n.709+270C=
ENST00000630236.2:c.*477C=	ENSP00000486766.1:n.*477C=
NM_001018078.2:c.1603C=	NP_001018088.1:p.Leu535=
NM_001288803.1:c.1675C=	NP_001275732.1:p.Leu559=
NM_004957.5:c.1753C=	NP_004948.4:p.Leu585=
NR_110170.1:n.1801C=
XM_005251864.2:c.1483+270C=	XP_005251921.1:n.1483+270C=
XM_011518437.1:c.1603C=	XP_011516739.1:p.Leu535=
XM_011518438.1:c.1603C=	XP_011516740.1:p.Leu535=
XM_011518439.1:c.910C=	XP_011516741.1:p.Leu304=
XR_242581.2:n.1650C=
XR_242582.2:n.1380+270C=
XM_005251864.4:c.1483+270C=	XP_005251921.1:n.1483+270C=
XM_011518439.2:c.910C=	XP_011516741.1:p.Leu304=
XM_017014565.2:c.1333+270C=	XP_016870054.1:n.1333+270C=
XM_017014566.1:c.910C=	XP_016870055.1:p.Leu304=
XR_242581.4:n.1648C=
XR_242582.4:n.1378+270C=
NM_004957.6:c.1753C= MANE Select	NP_004948.4:p.Leu585=