Canonical Allele Identifier: CA2691803946
Gene: FPGS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127813689del , CM000671.2:g.127813689del GRCh38
NC_000009.11:g.130575968del , CM000671.1:g.130575968del GRCh37
NC_000009.10:g.129615789del NCBI36
NG_009551.1:g.46084del , LRG_589:g.46084del
NG_023245.1:g.15815del

Transcript Alleles

HGVS Amino-acid change
ENST00000373247.7:c.*85del MANE Select ENSP00000362344.2:n.*85del
ENST00000373225.7:c.*85del ENSP00000362322.3:n.*85del
ENST00000373247.6:c.*85del ENSP00000362344.2:n.*85del
ENST00000393706.6:c.*85del ENSP00000377309.2:n.*85del
ENST00000460181.5:n.1837del
ENST00000467826.5:n.709+366del
ENST00000630236.2:c.*573del ENSP00000486766.1:n.*573del
NM_001018078.2:c.*85del NP_001018088.1:n.*85del
NM_001288803.1:c.*85del NP_001275732.1:n.*85del
NM_004957.5:c.*85del NP_004948.4:n.*85del
NR_110170.1:n.1897del
XM_005251864.2:c.1483+366del XP_005251921.1:n.1483+366del
XM_011518437.1:c.*85del XP_011516739.1:n.*85del
XM_011518438.1:c.*85del XP_011516740.1:n.*85del
XM_011518439.1:c.*85del XP_011516741.1:n.*85del
XR_242581.2:n.1746del
XR_242582.2:n.1380+366del
XM_005251864.4:c.1483+366del XP_005251921.1:n.1483+366del
XM_011518439.2:c.*85del XP_011516741.1:n.*85del
XM_017014565.2:c.1333+366del XP_016870054.1:n.1333+366del
XM_017014566.1:c.*85del XP_016870055.1:n.*85del
XR_242581.4:n.1744del
XR_242582.4:n.1378+366del
NM_004957.6:c.*85del MANE Select NP_004948.4:n.*85del