Canonical Allele Identifier: CA1879977112

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813420T= , CM000671.2:g.127813420T=	GRCh38
NC_000009.11:g.130575699T= , CM000671.1:g.130575699T=	GRCh37
NC_000009.10:g.129615520T=	NCBI36
NG_009551.1:g.46349A= , LRG_589:g.46349A=
NG_023245.1:g.15546T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.1580T= MANE Select	ENSP00000362344.2:p.Ile527=
ENST00000373225.7:c.1430T=	ENSP00000362322.3:p.Ile477=
ENST00000373228.5:c.*237T=	ENSP00000362325.1:n.*237T=
ENST00000373247.6:c.1580T=	ENSP00000362344.2:p.Ile527=
ENST00000393706.6:c.1502T=	ENSP00000377309.2:p.Ile501=
ENST00000460181.5:n.1568T=
ENST00000467826.5:n.709+97T=
ENST00000475270.1:n.406T=
ENST00000630236.2:c.*304T=	ENSP00000486766.1:n.*304T=
NM_001018078.2:c.1430T=	NP_001018088.1:p.Ile477=
NM_001288803.1:c.1502T=	NP_001275732.1:p.Ile501=
NM_004957.5:c.1580T=	NP_004948.4:p.Ile527=
NR_110170.1:n.1628T=
XM_005251864.2:c.1483+97T=	XP_005251921.1:n.1483+97T=
XM_011518437.1:c.1430T=	XP_011516739.1:p.Ile477=
XM_011518438.1:c.1430T=	XP_011516740.1:p.Ile477=
XM_011518439.1:c.737T=	XP_011516741.1:p.Ile246=
XR_242581.2:n.1477T=
XR_242582.2:n.1380+97T=
XM_005251864.4:c.1483+97T=	XP_005251921.1:n.1483+97T=
XM_011518439.2:c.737T=	XP_011516741.1:p.Ile246=
XM_017014565.2:c.1333+97T=	XP_016870054.1:n.1333+97T=
XM_017014566.1:c.737T=	XP_016870055.1:p.Ile246=
XR_242581.4:n.1475T=
XR_242582.4:n.1378+97T=
NM_004957.6:c.1580T= MANE Select	NP_004948.4:p.Ile527=