Canonical Allele Identifier: CA1879977545

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813723G= , CM000671.2:g.127813723G=	GRCh38
NC_000009.11:g.130576002G= , CM000671.1:g.130576002G=	GRCh37
NC_000009.10:g.129615823G=	NCBI36
NG_009551.1:g.46046C= , LRG_589:g.46046C=
NG_023245.1:g.15849G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*119G= MANE Select	ENSP00000362344.2:n.*119G=
ENST00000373225.7:c.*119G=	ENSP00000362322.3:n.*119G=
ENST00000373247.6:c.*119G=	ENSP00000362344.2:n.*119G=
ENST00000393706.6:c.*119G=	ENSP00000377309.2:n.*119G=
ENST00000460181.5:n.1871G=
ENST00000467826.5:n.709+400G=
ENST00000630236.2:c.*607G=	ENSP00000486766.1:n.*607G=
NM_001018078.2:c.*119G=	NP_001018088.1:n.*119G=
NM_001288803.1:c.*119G=	NP_001275732.1:n.*119G=
NM_004957.5:c.*119G=	NP_004948.4:n.*119G=
NR_110170.1:n.1931G=
XM_005251864.2:c.1483+400G=	XP_005251921.1:n.1483+400G=
XM_011518437.1:c.*119G=	XP_011516739.1:n.*119G=
XM_011518438.1:c.*119G=	XP_011516740.1:n.*119G=
XM_011518439.1:c.*119G=	XP_011516741.1:n.*119G=
XR_242581.2:n.1780G=
XR_242582.2:n.1380+400G=
XM_005251864.4:c.1483+400G=	XP_005251921.1:n.1483+400G=
XM_011518439.2:c.*119G=	XP_011516741.1:n.*119G=
XM_017014565.2:c.1333+400G=	XP_016870054.1:n.1333+400G=
XM_017014566.1:c.*119G=	XP_016870055.1:n.*119G=
XR_242581.4:n.1778G=
XR_242582.4:n.1378+400G=
NM_004957.6:c.*119G= MANE Select	NP_004948.4:n.*119G=