Canonical Allele Identifier: CA1879977692

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813825G= , CM000671.2:g.127813825G=	GRCh38
NC_000009.11:g.130576104G= , CM000671.1:g.130576104G=	GRCh37
NC_000009.10:g.129615925G=	NCBI36
NG_009551.1:g.45944C= , LRG_589:g.45944C=
NG_023245.1:g.15951G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*221G= MANE Select	ENSP00000362344.2:n.*221G=
ENST00000373225.7:c.*221G=	ENSP00000362322.3:n.*221G=
ENST00000373247.6:c.*221G=	ENSP00000362344.2:n.*221G=
ENST00000393706.6:c.*221G=	ENSP00000377309.2:n.*221G=
ENST00000460181.5:n.1973G=
ENST00000467826.5:n.710-383G=
ENST00000630236.2:c.*709G=	ENSP00000486766.1:n.*709G=
NM_001018078.2:c.*221G=	NP_001018088.1:n.*221G=
NM_001288803.1:c.*221G=	NP_001275732.1:n.*221G=
NM_004957.5:c.*221G=	NP_004948.4:n.*221G=
NR_110170.1:n.2033G=
XM_005251864.2:c.1484-383G=	XP_005251921.1:n.1484-383G=
XM_011518437.1:c.*221G=	XP_011516739.1:n.*221G=
XM_011518438.1:c.*221G=	XP_011516740.1:n.*221G=
XM_011518439.1:c.*221G=	XP_011516741.1:n.*221G=
XR_242581.2:n.1882G=
XR_242582.2:n.1381-383G=
XM_005251864.4:c.1484-383G=	XP_005251921.1:n.1484-383G=
XM_011518439.2:c.*221G=	XP_011516741.1:n.*221G=
XM_017014565.2:c.1334-383G=	XP_016870054.1:n.1334-383G=
XM_017014566.1:c.*221G=	XP_016870055.1:n.*221G=
XR_242581.4:n.1880G=
XR_242582.4:n.1379-383G=
NM_004957.6:c.*221G= MANE Select	NP_004948.4:n.*221G=