Canonical Allele Identifier: CA2691803964

Gene: FPGS

Linked Data

• gnomAD v4: 9-127813715-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813715G>T , CM000671.2:g.127813715G>T	GRCh38
NC_000009.11:g.130575994G>T , CM000671.1:g.130575994G>T	GRCh37
NC_000009.10:g.129615815G>T	NCBI36
NG_009551.1:g.46054C>A , LRG_589:g.46054C>A
NG_023245.1:g.15841G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*111G>T MANE Select	ENSP00000362344.2:n.*111G>T
ENST00000373225.7:c.*111G>T	ENSP00000362322.3:n.*111G>T
ENST00000373247.6:c.*111G>T	ENSP00000362344.2:n.*111G>T
ENST00000393706.6:c.*111G>T	ENSP00000377309.2:n.*111G>T
ENST00000460181.5:n.1863G>T
ENST00000467826.5:n.709+392G>T
ENST00000630236.2:c.*599G>T	ENSP00000486766.1:n.*599G>T
NM_001018078.2:c.*111G>T	NP_001018088.1:n.*111G>T
NM_001288803.1:c.*111G>T	NP_001275732.1:n.*111G>T
NM_004957.5:c.*111G>T	NP_004948.4:n.*111G>T
NR_110170.1:n.1923G>T
XM_005251864.2:c.1483+392G>T	XP_005251921.1:n.1483+392G>T
XM_011518437.1:c.*111G>T	XP_011516739.1:n.*111G>T
XM_011518438.1:c.*111G>T	XP_011516740.1:n.*111G>T
XM_011518439.1:c.*111G>T	XP_011516741.1:n.*111G>T
XR_242581.2:n.1772G>T
XR_242582.2:n.1380+392G>T
XM_005251864.4:c.1483+392G>T	XP_005251921.1:n.1483+392G>T
XM_011518439.2:c.*111G>T	XP_011516741.1:n.*111G>T
XM_017014565.2:c.1333+392G>T	XP_016870054.1:n.1333+392G>T
XM_017014566.1:c.*111G>T	XP_016870055.1:n.*111G>T
XR_242581.4:n.1770G>T
XR_242582.4:n.1378+392G>T
NM_004957.6:c.*111G>T MANE Select	NP_004948.4:n.*111G>T