Canonical Allele Identifier: CA1879977897

Gene: FPGS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813948_127813949delinsTG , CM000671.2:g.127813948_127813949delinsTG	GRCh38
NC_000009.11:g.130576227_130576228delinsTG , CM000671.1:g.130576227_130576228delinsTG	GRCh37
NC_000009.10:g.129616048_129616049delinsTG	NCBI36
NG_009551.1:g.45820_45821delinsCA , LRG_589:g.45820_45821delinsCA
NG_023245.1:g.16074_16075delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*344_*345delinsTG MANE Select	ENSP00000362344.2:n.*344_*345delinsTG
ENST00000373225.7:c.*344_*345delinsTG	ENSP00000362322.3:n.*344_*345delinsTG
ENST00000373247.6:c.*344_*345delinsTG	ENSP00000362344.2:n.*344_*345delinsTG
ENST00000393706.6:c.*344_*345delinsTG	ENSP00000377309.2:n.*344_*345delinsTG
ENST00000460181.5:n.2096_2097delinsTG
ENST00000467826.5:n.710-260_710-259delinsTG
ENST00000630236.2:c.*832_*833delinsTG	ENSP00000486766.1:n.*832_*833delinsTG
NM_001018078.2:c.*344_*345delinsTG	NP_001018088.1:n.*344_*345delinsTG
NM_001288803.1:c.*344_*345delinsTG	NP_001275732.1:n.*344_*345delinsTG
NM_004957.5:c.*344_*345delinsTG	NP_004948.4:n.*344_*345delinsTG
NR_110170.1:n.2156_2157delinsTG
XM_005251864.2:c.1484-260_1484-259delinsTG	XP_005251921.1:n.1484-260_1484-259delinsTG
XM_011518437.1:c.*344_*345delinsTG	XP_011516739.1:n.*344_*345delinsTG
XM_011518438.1:c.*344_*345delinsTG	XP_011516740.1:n.*344_*345delinsTG
XM_011518439.1:c.*344_*345delinsTG	XP_011516741.1:n.*344_*345delinsTG
XR_242581.2:n.2005_2006delinsTG
XR_242582.2:n.1381-260_1381-259delinsTG
XM_005251864.4:c.1484-260_1484-259delinsTG	XP_005251921.1:n.1484-260_1484-259delinsTG
XM_011518439.2:c.*344_*345delinsTG	XP_011516741.1:n.*344_*345delinsTG
XM_017014565.2:c.1334-260_1334-259delinsTG	XP_016870054.1:n.1334-260_1334-259delinsTG
XM_017014566.1:c.*344_*345delinsTG	XP_016870055.1:n.*344_*345delinsTG
XR_242581.4:n.2003_2004delinsTG
XR_242582.4:n.1379-260_1379-259delinsTG
NM_004957.6:c.*344_*345delinsTG MANE Select	NP_004948.4:n.*344_*345delinsTG