Canonical Allele Identifier: CA2691804162

Gene: FPGS

Linked Data

• gnomAD v4: 9-127813867-CCCAACACCCCGCCTGCCTCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813868_127813888del , CM000671.2:g.127813868_127813888del	GRCh38
NC_000009.11:g.130576147_130576167del , CM000671.1:g.130576147_130576167del	GRCh37
NC_000009.10:g.129615968_129615988del	NCBI36
NG_009551.1:g.45881_45901del , LRG_589:g.45881_45901del
NG_023245.1:g.15994_16014del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*264_*284del MANE Select	ENSP00000362344.2:n.*264_*284del
ENST00000373225.7:c.*264_*284del	ENSP00000362322.3:n.*264_*284del
ENST00000373247.6:c.*264_*284del	ENSP00000362344.2:n.*264_*284del
ENST00000393706.6:c.*264_*284del	ENSP00000377309.2:n.*264_*284del
ENST00000460181.5:n.2016_2036del
ENST00000467826.5:n.710-340_710-320del
ENST00000630236.2:c.*752_*772del	ENSP00000486766.1:n.*752_*772del
NM_001018078.2:c.*264_*284del	NP_001018088.1:n.*264_*284del
NM_001288803.1:c.*264_*284del	NP_001275732.1:n.*264_*284del
NM_004957.5:c.*264_*284del	NP_004948.4:n.*264_*284del
NR_110170.1:n.2076_2096del
XM_005251864.2:c.1484-340_1484-320del	XP_005251921.1:n.1484-340_1484-320del
XM_011518437.1:c.*264_*284del	XP_011516739.1:n.*264_*284del
XM_011518438.1:c.*264_*284del	XP_011516740.1:n.*264_*284del
XM_011518439.1:c.*264_*284del	XP_011516741.1:n.*264_*284del
XR_242581.2:n.1925_1945del
XR_242582.2:n.1381-340_1381-320del
XM_005251864.4:c.1484-340_1484-320del	XP_005251921.1:n.1484-340_1484-320del
XM_011518439.2:c.*264_*284del	XP_011516741.1:n.*264_*284del
XM_017014565.2:c.1334-340_1334-320del	XP_016870054.1:n.1334-340_1334-320del
XM_017014566.1:c.*264_*284del	XP_016870055.1:n.*264_*284del
XR_242581.4:n.1923_1943del
XR_242582.4:n.1379-340_1379-320del
NM_004957.6:c.*264_*284del MANE Select	NP_004948.4:n.*264_*284del