Canonical Allele Identifier: CA1879977432

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813613_127813614delinsCG , CM000671.2:g.127813613_127813614delinsCG	GRCh38
NC_000009.11:g.130575892_130575893delinsCG , CM000671.1:g.130575892_130575893delinsCG	GRCh37
NC_000009.10:g.129615713_129615714delinsCG	NCBI36
NG_009551.1:g.46155_46156delinsCG , LRG_589:g.46155_46156delinsCG
NG_023245.1:g.15739_15740delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*9_*10delinsCG MANE Select	ENSP00000362344.2:n.*9_*10delinsCG
ENST00000373225.7:c.*9_*10delinsCG	ENSP00000362322.3:n.*9_*10delinsCG
ENST00000373247.6:c.*9_*10delinsCG	ENSP00000362344.2:n.*9_*10delinsCG
ENST00000393706.6:c.*9_*10delinsCG	ENSP00000377309.2:n.*9_*10delinsCG
ENST00000460181.5:n.1761_1762delinsCG
ENST00000467826.5:n.709+290_709+291delinsCG
ENST00000630236.2:c.*497_*498delinsCG	ENSP00000486766.1:n.*497_*498delinsCG
NM_001018078.2:c.*9_*10delinsCG	NP_001018088.1:n.*9_*10delinsCG
NM_001288803.1:c.*9_*10delinsCG	NP_001275732.1:n.*9_*10delinsCG
NM_004957.5:c.*9_*10delinsCG	NP_004948.4:n.*9_*10delinsCG
NR_110170.1:n.1821_1822delinsCG
XM_005251864.2:c.1483+290_1483+291delinsCG	XP_005251921.1:n.1483+290_1483+291delinsCG
XM_011518437.1:c.*9_*10delinsCG	XP_011516739.1:n.*9_*10delinsCG
XM_011518438.1:c.*9_*10delinsCG	XP_011516740.1:n.*9_*10delinsCG
XM_011518439.1:c.*9_*10delinsCG	XP_011516741.1:n.*9_*10delinsCG
XR_242581.2:n.1670_1671delinsCG
XR_242582.2:n.1380+290_1380+291delinsCG
XM_005251864.4:c.1483+290_1483+291delinsCG	XP_005251921.1:n.1483+290_1483+291delinsCG
XM_011518439.2:c.*9_*10delinsCG	XP_011516741.1:n.*9_*10delinsCG
XM_017014565.2:c.1333+290_1333+291delinsCG	XP_016870054.1:n.1333+290_1333+291delinsCG
XM_017014566.1:c.*9_*10delinsCG	XP_016870055.1:n.*9_*10delinsCG
XR_242581.4:n.1668_1669delinsCG
XR_242582.4:n.1378+290_1378+291delinsCG
NM_004957.6:c.*9_*10delinsCG MANE Select	NP_004948.4:n.*9_*10delinsCG