Canonical Allele Identifier: CA1879977678

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813821C= , CM000671.2:g.127813821C=	GRCh38
NC_000009.11:g.130576100C= , CM000671.1:g.130576100C=	GRCh37
NC_000009.10:g.129615921C=	NCBI36
NG_009551.1:g.45948G= , LRG_589:g.45948G=
NG_023245.1:g.15947C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*217C= MANE Select	ENSP00000362344.2:n.*217C=
ENST00000373225.7:c.*217C=	ENSP00000362322.3:n.*217C=
ENST00000373247.6:c.*217C=	ENSP00000362344.2:n.*217C=
ENST00000393706.6:c.*217C=	ENSP00000377309.2:n.*217C=
ENST00000460181.5:n.1969C=
ENST00000467826.5:n.710-387C=
ENST00000630236.2:c.*705C=	ENSP00000486766.1:n.*705C=
NM_001018078.2:c.*217C=	NP_001018088.1:n.*217C=
NM_001288803.1:c.*217C=	NP_001275732.1:n.*217C=
NM_004957.5:c.*217C=	NP_004948.4:n.*217C=
NR_110170.1:n.2029C=
XM_005251864.2:c.1484-387C=	XP_005251921.1:n.1484-387C=
XM_011518437.1:c.*217C=	XP_011516739.1:n.*217C=
XM_011518438.1:c.*217C=	XP_011516740.1:n.*217C=
XM_011518439.1:c.*217C=	XP_011516741.1:n.*217C=
XR_242581.2:n.1878C=
XR_242582.2:n.1381-387C=
XM_005251864.4:c.1484-387C=	XP_005251921.1:n.1484-387C=
XM_011518439.2:c.*217C=	XP_011516741.1:n.*217C=
XM_017014565.2:c.1334-387C=	XP_016870054.1:n.1334-387C=
XM_017014566.1:c.*217C=	XP_016870055.1:n.*217C=
XR_242581.4:n.1876C=
XR_242582.4:n.1379-387C=
NM_004957.6:c.*217C= MANE Select	NP_004948.4:n.*217C=