Canonical Allele Identifier: CA1879977835

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813897C= , CM000671.2:g.127813897C=	GRCh38
NC_000009.11:g.130576176C= , CM000671.1:g.130576176C=	GRCh37
NC_000009.10:g.129615997C=	NCBI36
NG_009551.1:g.45872G= , LRG_589:g.45872G=
NG_023245.1:g.16023C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*293C= MANE Select	ENSP00000362344.2:n.*293C=
ENST00000373225.7:c.*293C=	ENSP00000362322.3:n.*293C=
ENST00000373247.6:c.*293C=	ENSP00000362344.2:n.*293C=
ENST00000393706.6:c.*293C=	ENSP00000377309.2:n.*293C=
ENST00000460181.5:n.2045C=
ENST00000467826.5:n.710-311C=
ENST00000630236.2:c.*781C=	ENSP00000486766.1:n.*781C=
NM_001018078.2:c.*293C=	NP_001018088.1:n.*293C=
NM_001288803.1:c.*293C=	NP_001275732.1:n.*293C=
NM_004957.5:c.*293C=	NP_004948.4:n.*293C=
NR_110170.1:n.2105C=
XM_005251864.2:c.1484-311C=	XP_005251921.1:n.1484-311C=
XM_011518437.1:c.*293C=	XP_011516739.1:n.*293C=
XM_011518438.1:c.*293C=	XP_011516740.1:n.*293C=
XM_011518439.1:c.*293C=	XP_011516741.1:n.*293C=
XR_242581.2:n.1954C=
XR_242582.2:n.1381-311C=
XM_005251864.4:c.1484-311C=	XP_005251921.1:n.1484-311C=
XM_011518439.2:c.*293C=	XP_011516741.1:n.*293C=
XM_017014565.2:c.1334-311C=	XP_016870054.1:n.1334-311C=
XM_017014566.1:c.*293C=	XP_016870055.1:n.*293C=
XR_242581.4:n.1952C=
XR_242582.4:n.1379-311C=
NM_004957.6:c.*293C= MANE Select	NP_004948.4:n.*293C=