Canonical Allele Identifier: CA2691803955

Gene: FPGS

Linked Data

• gnomAD v4: 9-127813705-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813705G>A , CM000671.2:g.127813705G>A	GRCh38
NC_000009.11:g.130575984G>A , CM000671.1:g.130575984G>A	GRCh37
NC_000009.10:g.129615805G>A	NCBI36
NG_009551.1:g.46064C>T , LRG_589:g.46064C>T
NG_023245.1:g.15831G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*101G>A MANE Select	ENSP00000362344.2:n.*101G>A
ENST00000373225.7:c.*101G>A	ENSP00000362322.3:n.*101G>A
ENST00000373247.6:c.*101G>A	ENSP00000362344.2:n.*101G>A
ENST00000393706.6:c.*101G>A	ENSP00000377309.2:n.*101G>A
ENST00000460181.5:n.1853G>A
ENST00000467826.5:n.709+382G>A
ENST00000630236.2:c.*589G>A	ENSP00000486766.1:n.*589G>A
NM_001018078.2:c.*101G>A	NP_001018088.1:n.*101G>A
NM_001288803.1:c.*101G>A	NP_001275732.1:n.*101G>A
NM_004957.5:c.*101G>A	NP_004948.4:n.*101G>A
NR_110170.1:n.1913G>A
XM_005251864.2:c.1483+382G>A	XP_005251921.1:n.1483+382G>A
XM_011518437.1:c.*101G>A	XP_011516739.1:n.*101G>A
XM_011518438.1:c.*101G>A	XP_011516740.1:n.*101G>A
XM_011518439.1:c.*101G>A	XP_011516741.1:n.*101G>A
XR_242581.2:n.1762G>A
XR_242582.2:n.1380+382G>A
XM_005251864.4:c.1483+382G>A	XP_005251921.1:n.1483+382G>A
XM_011518439.2:c.*101G>A	XP_011516741.1:n.*101G>A
XM_017014565.2:c.1333+382G>A	XP_016870054.1:n.1333+382G>A
XM_017014566.1:c.*101G>A	XP_016870055.1:n.*101G>A
XR_242581.4:n.1760G>A
XR_242582.4:n.1378+382G>A
NM_004957.6:c.*101G>A MANE Select	NP_004948.4:n.*101G>A