Canonical Allele Identifier: CA860217922

Gene: FPGS

Linked Data

• dbSNP Id: rs1181263277
• gnomAD v4: 9-127813908-G-T
• MyVariant Identifiers: chr9:g.130576187G>T (hg19) ; chr9:g.127813908G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813908G>T , CM000671.2:g.127813908G>T	GRCh38
NC_000009.11:g.130576187G>T , CM000671.1:g.130576187G>T	GRCh37
NC_000009.10:g.129616008G>T	NCBI36
NG_009551.1:g.45861C>A , LRG_589:g.45861C>A
NG_023245.1:g.16034G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373247.7:c.*304G>T MANE Select	ENSP00000362344.2:n.*304G>T
ENST00000373225.7:c.*304G>T	ENSP00000362322.3:n.*304G>T
ENST00000373247.6:c.*304G>T	ENSP00000362344.2:n.*304G>T
ENST00000393706.6:c.*304G>T	ENSP00000377309.2:n.*304G>T
ENST00000460181.5:n.2056G>T
ENST00000467826.5:n.710-300G>T
ENST00000630236.2:c.*792G>T	ENSP00000486766.1:n.*792G>T
NM_001018078.2:c.*304G>T	NP_001018088.1:n.*304G>T
NM_001288803.1:c.*304G>T	NP_001275732.1:n.*304G>T
NM_004957.5:c.*304G>T	NP_004948.4:n.*304G>T
NR_110170.1:n.2116G>T
XM_005251864.2:c.1484-300G>T	XP_005251921.1:n.1484-300G>T
XM_011518437.1:c.*304G>T	XP_011516739.1:n.*304G>T
XM_011518438.1:c.*304G>T	XP_011516740.1:n.*304G>T
XM_011518439.1:c.*304G>T	XP_011516741.1:n.*304G>T
XR_242581.2:n.1965G>T
XR_242582.2:n.1381-300G>T
XM_005251864.4:c.1484-300G>T	XP_005251921.1:n.1484-300G>T
XM_011518439.2:c.*304G>T	XP_011516741.1:n.*304G>T
XM_017014565.2:c.1334-300G>T	XP_016870054.1:n.1334-300G>T
XM_017014566.1:c.*304G>T	XP_016870055.1:n.*304G>T
XR_242581.4:n.1963G>T
XR_242582.4:n.1379-300G>T
NM_004957.6:c.*304G>T MANE Select	NP_004948.4:n.*304G>T