Canonical Allele Identifier: CA1879977728
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127813851C= , CM000671.2:g.127813851C= GRCh38
NC_000009.11:g.130576130C= , CM000671.1:g.130576130C= GRCh37
NC_000009.10:g.129615951C= NCBI36
NG_009551.1:g.45918G= , LRG_589:g.45918G=
NG_023245.1:g.15977C=

Transcript Alleles

HGVS Amino-acid change
ENST00000373247.7:c.*247C= MANE Select ENSP00000362344.2:n.*247C=
ENST00000373225.7:c.*247C= ENSP00000362322.3:n.*247C=
ENST00000373247.6:c.*247C= ENSP00000362344.2:n.*247C=
ENST00000393706.6:c.*247C= ENSP00000377309.2:n.*247C=
ENST00000460181.5:n.1999C=
ENST00000467826.5:n.710-357C=
ENST00000630236.2:c.*735C= ENSP00000486766.1:n.*735C=
NM_001018078.2:c.*247C= NP_001018088.1:n.*247C=
NM_001288803.1:c.*247C= NP_001275732.1:n.*247C=
NM_004957.5:c.*247C= NP_004948.4:n.*247C=
NR_110170.1:n.2059C=
XM_005251864.2:c.1484-357C= XP_005251921.1:n.1484-357C=
XM_011518437.1:c.*247C= XP_011516739.1:n.*247C=
XM_011518438.1:c.*247C= XP_011516740.1:n.*247C=
XM_011518439.1:c.*247C= XP_011516741.1:n.*247C=
XR_242581.2:n.1908C=
XR_242582.2:n.1381-357C=
XM_005251864.4:c.1484-357C= XP_005251921.1:n.1484-357C=
XM_011518439.2:c.*247C= XP_011516741.1:n.*247C=
XM_017014565.2:c.1334-357C= XP_016870054.1:n.1334-357C=
XM_017014566.1:c.*247C= XP_016870055.1:n.*247C=
XR_242581.4:n.1906C=
XR_242582.4:n.1379-357C=
NM_004957.6:c.*247C= MANE Select NP_004948.4:n.*247C=