Canonical Allele Identifier: CA2691803907

Gene: FPGS

Linked Data

• gnomAD v4: 9-127813642-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127813642T>C , CM000671.2:g.127813642T>C	GRCh38
NC_000009.11:g.130575921T>C , CM000671.1:g.130575921T>C	GRCh37
NC_000009.10:g.129615742T>C	NCBI36
NG_009551.1:g.46127A>G , LRG_589:g.46127A>G
NG_023245.1:g.15768T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373247.7:c.*38T>C MANE Select	ENSP00000362344.2:n.*38T>C
ENST00000373225.7:c.*38T>C	ENSP00000362322.3:n.*38T>C
ENST00000373247.6:c.*38T>C	ENSP00000362344.2:n.*38T>C
ENST00000393706.6:c.*38T>C	ENSP00000377309.2:n.*38T>C
ENST00000460181.5:n.1790T>C
ENST00000467826.5:n.709+319T>C
ENST00000630236.2:c.*526T>C	ENSP00000486766.1:n.*526T>C
NM_001018078.2:c.*38T>C	NP_001018088.1:n.*38T>C
NM_001288803.1:c.*38T>C	NP_001275732.1:n.*38T>C
NM_004957.5:c.*38T>C	NP_004948.4:n.*38T>C
NR_110170.1:n.1850T>C
XM_005251864.2:c.1483+319T>C	XP_005251921.1:n.1483+319T>C
XM_011518437.1:c.*38T>C	XP_011516739.1:n.*38T>C
XM_011518438.1:c.*38T>C	XP_011516740.1:n.*38T>C
XM_011518439.1:c.*38T>C	XP_011516741.1:n.*38T>C
XR_242581.2:n.1699T>C
XR_242582.2:n.1380+319T>C
XM_005251864.4:c.1483+319T>C	XP_005251921.1:n.1483+319T>C
XM_011518439.2:c.*38T>C	XP_011516741.1:n.*38T>C
XM_017014565.2:c.1333+319T>C	XP_016870054.1:n.1333+319T>C
XM_017014566.1:c.*38T>C	XP_016870055.1:n.*38T>C
XR_242581.4:n.1697T>C
XR_242582.4:n.1378+319T>C
NM_004957.6:c.*38T>C MANE Select	NP_004948.4:n.*38T>C