Canonical Allele Identifier: CA1879977598

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813764T= , CM000671.2:g.127813764T=	GRCh38
NC_000009.11:g.130576043T= , CM000671.1:g.130576043T=	GRCh37
NC_000009.10:g.129615864T=	NCBI36
NG_009551.1:g.46005A= , LRG_589:g.46005A=
NG_023245.1:g.15890T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*160T= MANE Select	ENSP00000362344.2:n.*160T=
ENST00000373225.7:c.*160T=	ENSP00000362322.3:n.*160T=
ENST00000373247.6:c.*160T=	ENSP00000362344.2:n.*160T=
ENST00000393706.6:c.*160T=	ENSP00000377309.2:n.*160T=
ENST00000460181.5:n.1912T=
ENST00000467826.5:n.709+441T=
ENST00000630236.2:c.*648T=	ENSP00000486766.1:n.*648T=
NM_001018078.2:c.*160T=	NP_001018088.1:n.*160T=
NM_001288803.1:c.*160T=	NP_001275732.1:n.*160T=
NM_004957.5:c.*160T=	NP_004948.4:n.*160T=
NR_110170.1:n.1972T=
XM_005251864.2:c.1483+441T=	XP_005251921.1:n.1483+441T=
XM_011518437.1:c.*160T=	XP_011516739.1:n.*160T=
XM_011518438.1:c.*160T=	XP_011516740.1:n.*160T=
XM_011518439.1:c.*160T=	XP_011516741.1:n.*160T=
XR_242581.2:n.1821T=
XR_242582.2:n.1380+441T=
XM_005251864.4:c.1483+441T=	XP_005251921.1:n.1483+441T=
XM_011518439.2:c.*160T=	XP_011516741.1:n.*160T=
XM_017014565.2:c.1333+441T=	XP_016870054.1:n.1333+441T=
XM_017014566.1:c.*160T=	XP_016870055.1:n.*160T=
XR_242581.4:n.1819T=
XR_242582.4:n.1378+441T=
NM_004957.6:c.*160T= MANE Select	NP_004948.4:n.*160T=