Canonical Allele Identifier: CA2691803999

Gene: FPGS

Linked Data

• gnomAD v4: 9-127813756-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813756T>G , CM000671.2:g.127813756T>G	GRCh38
NC_000009.11:g.130576035T>G , CM000671.1:g.130576035T>G	GRCh37
NC_000009.10:g.129615856T>G	NCBI36
NG_009551.1:g.46013A>C , LRG_589:g.46013A>C
NG_023245.1:g.15882T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*152T>G MANE Select	ENSP00000362344.2:n.*152T>G
ENST00000373225.7:c.*152T>G	ENSP00000362322.3:n.*152T>G
ENST00000373247.6:c.*152T>G	ENSP00000362344.2:n.*152T>G
ENST00000393706.6:c.*152T>G	ENSP00000377309.2:n.*152T>G
ENST00000460181.5:n.1904T>G
ENST00000467826.5:n.709+433T>G
ENST00000630236.2:c.*640T>G	ENSP00000486766.1:n.*640T>G
NM_001018078.2:c.*152T>G	NP_001018088.1:n.*152T>G
NM_001288803.1:c.*152T>G	NP_001275732.1:n.*152T>G
NM_004957.5:c.*152T>G	NP_004948.4:n.*152T>G
NR_110170.1:n.1964T>G
XM_005251864.2:c.1483+433T>G	XP_005251921.1:n.1483+433T>G
XM_011518437.1:c.*152T>G	XP_011516739.1:n.*152T>G
XM_011518438.1:c.*152T>G	XP_011516740.1:n.*152T>G
XM_011518439.1:c.*152T>G	XP_011516741.1:n.*152T>G
XR_242581.2:n.1813T>G
XR_242582.2:n.1380+433T>G
XM_005251864.4:c.1483+433T>G	XP_005251921.1:n.1483+433T>G
XM_011518439.2:c.*152T>G	XP_011516741.1:n.*152T>G
XM_017014565.2:c.1333+433T>G	XP_016870054.1:n.1333+433T>G
XM_017014566.1:c.*152T>G	XP_016870055.1:n.*152T>G
XR_242581.4:n.1811T>G
XR_242582.4:n.1378+433T>G
NM_004957.6:c.*152T>G MANE Select	NP_004948.4:n.*152T>G