Canonical Allele Identifier: CA1879976959

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813354A= , CM000671.2:g.127813354A=	GRCh38
NC_000009.11:g.130575633A= , CM000671.1:g.130575633A=	GRCh37
NC_000009.10:g.129615454A=	NCBI36
NG_009551.1:g.46415T= , LRG_589:g.46415T=
NG_023245.1:g.15480A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1514A= MANE Select	ENSP00000362344.2:p.His505=
ENST00000373225.7:c.1364A=	ENSP00000362322.3:p.His455=
ENST00000373228.5:c.*171A=	ENSP00000362325.1:n.*171A=
ENST00000373247.6:c.1514A=	ENSP00000362344.2:p.His505=
ENST00000393706.6:c.1436A=	ENSP00000377309.2:p.His479=
ENST00000460181.5:n.1502A=
ENST00000467826.5:n.709+31A=
ENST00000475270.1:n.340A=
ENST00000630236.2:c.*238A=	ENSP00000486766.1:n.*238A=
NM_001018078.2:c.1364A=	NP_001018088.1:p.His455=
NM_001288803.1:c.1436A=	NP_001275732.1:p.His479=
NM_004957.5:c.1514A=	NP_004948.4:p.His505=
NR_110170.1:n.1562A=
XM_005251864.2:c.1483+31A=	XP_005251921.1:n.1483+31A=
XM_011518437.1:c.1364A=	XP_011516739.1:p.His455=
XM_011518438.1:c.1364A=	XP_011516740.1:p.His455=
XM_011518439.1:c.671A=	XP_011516741.1:p.His224=
XR_242581.2:n.1411A=
XR_242582.2:n.1380+31A=
XM_005251864.4:c.1483+31A=	XP_005251921.1:n.1483+31A=
XM_011518439.2:c.671A=	XP_011516741.1:p.His224=
XM_017014565.2:c.1333+31A=	XP_016870054.1:n.1333+31A=
XM_017014566.1:c.671A=	XP_016870055.1:p.His224=
XR_242581.4:n.1409A=
XR_242582.4:n.1378+31A=
NM_004957.6:c.1514A= MANE Select	NP_004948.4:p.His505=