Canonical Allele Identifier: CA2691804335

Gene: FPGS

Linked Data

• gnomAD v4: 9-127814000-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127814000G>T , CM000671.2:g.127814000G>T	GRCh38
NC_000009.11:g.130576279G>T , CM000671.1:g.130576279G>T	GRCh37
NC_000009.10:g.129616100G>T	NCBI36
NG_009551.1:g.45769C>A , LRG_589:g.45769C>A
NG_023245.1:g.16126G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*396G>T MANE Select	ENSP00000362344.2:n.*396G>T
ENST00000373225.7:c.*396G>T	ENSP00000362322.3:n.*396G>T
ENST00000373247.6:c.*396G>T	ENSP00000362344.2:n.*396G>T
ENST00000393706.6:c.*396G>T	ENSP00000377309.2:n.*396G>T
ENST00000460181.5:n.2148G>T
ENST00000467826.5:n.710-208G>T
ENST00000630236.2:c.*884G>T	ENSP00000486766.1:n.*884G>T
NM_001018078.2:c.*396G>T	NP_001018088.1:n.*396G>T
NM_001288803.1:c.*396G>T	NP_001275732.1:n.*396G>T
NM_004957.5:c.*396G>T	NP_004948.4:n.*396G>T
NR_110170.1:n.2208G>T
XM_005251864.2:c.1484-208G>T	XP_005251921.1:n.1484-208G>T
XM_011518437.1:c.*396G>T	XP_011516739.1:n.*396G>T
XM_011518438.1:c.*396G>T	XP_011516740.1:n.*396G>T
XM_011518439.1:c.*396G>T	XP_011516741.1:n.*396G>T
XR_242581.2:n.2057G>T
XR_242582.2:n.1381-208G>T
XM_005251864.4:c.1484-208G>T	XP_005251921.1:n.1484-208G>T
XM_011518439.2:c.*396G>T	XP_011516741.1:n.*396G>T
XM_017014565.2:c.1334-208G>T	XP_016870054.1:n.1334-208G>T
XM_017014566.1:c.*396G>T	XP_016870055.1:n.*396G>T
XR_242581.4:n.2055G>T
XR_242582.4:n.1379-208G>T
NM_004957.6:c.*396G>T MANE Select	NP_004948.4:n.*396G>T