Canonical Allele Identifier: CA1879977591

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813759C= , CM000671.2:g.127813759C=	GRCh38
NC_000009.11:g.130576038C= , CM000671.1:g.130576038C=	GRCh37
NC_000009.10:g.129615859C=	NCBI36
NG_009551.1:g.46010G= , LRG_589:g.46010G=
NG_023245.1:g.15885C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*155C= MANE Select	ENSP00000362344.2:n.*155C=
ENST00000373225.7:c.*155C=	ENSP00000362322.3:n.*155C=
ENST00000373247.6:c.*155C=	ENSP00000362344.2:n.*155C=
ENST00000393706.6:c.*155C=	ENSP00000377309.2:n.*155C=
ENST00000460181.5:n.1907C=
ENST00000467826.5:n.709+436C=
ENST00000630236.2:c.*643C=	ENSP00000486766.1:n.*643C=
NM_001018078.2:c.*155C=	NP_001018088.1:n.*155C=
NM_001288803.1:c.*155C=	NP_001275732.1:n.*155C=
NM_004957.5:c.*155C=	NP_004948.4:n.*155C=
NR_110170.1:n.1967C=
XM_005251864.2:c.1483+436C=	XP_005251921.1:n.1483+436C=
XM_011518437.1:c.*155C=	XP_011516739.1:n.*155C=
XM_011518438.1:c.*155C=	XP_011516740.1:n.*155C=
XM_011518439.1:c.*155C=	XP_011516741.1:n.*155C=
XR_242581.2:n.1816C=
XR_242582.2:n.1380+436C=
XM_005251864.4:c.1483+436C=	XP_005251921.1:n.1483+436C=
XM_011518439.2:c.*155C=	XP_011516741.1:n.*155C=
XM_017014565.2:c.1333+436C=	XP_016870054.1:n.1333+436C=
XM_017014566.1:c.*155C=	XP_016870055.1:n.*155C=
XR_242581.4:n.1814C=
XR_242582.4:n.1378+436C=
NM_004957.6:c.*155C= MANE Select	NP_004948.4:n.*155C=