Canonical Allele Identifier: CA1879977589
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127813759_127813762delinsCTTT , CM000671.2:g.127813759_127813762delinsCTTT GRCh38
NC_000009.11:g.130576038_130576041delinsCTTT , CM000671.1:g.130576038_130576041delinsCTTT GRCh37
NC_000009.10:g.129615859_129615862delinsCTTT NCBI36
NG_009551.1:g.46007_46010delinsAAAG , LRG_589:g.46007_46010delinsAAAG
NG_023245.1:g.15885_15888delinsCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000373247.7:c.*155_*158delinsCTTT MANE Select ENSP00000362344.2:n.*155_*158delinsCTTT
ENST00000373225.7:c.*155_*158delinsCTTT ENSP00000362322.3:n.*155_*158delinsCTTT
ENST00000373247.6:c.*155_*158delinsCTTT ENSP00000362344.2:n.*155_*158delinsCTTT
ENST00000393706.6:c.*155_*158delinsCTTT ENSP00000377309.2:n.*155_*158delinsCTTT
ENST00000460181.5:n.1907_1910delinsCTTT
ENST00000467826.5:n.709+436_709+439delinsCTTT
ENST00000630236.2:c.*643_*646delinsCTTT ENSP00000486766.1:n.*643_*646delinsCTTT
NM_001018078.2:c.*155_*158delinsCTTT NP_001018088.1:n.*155_*158delinsCTTT
NM_001288803.1:c.*155_*158delinsCTTT NP_001275732.1:n.*155_*158delinsCTTT
NM_004957.5:c.*155_*158delinsCTTT NP_004948.4:n.*155_*158delinsCTTT
NR_110170.1:n.1967_1970delinsCTTT
XM_005251864.2:c.1483+436_1483+439delinsCTTT XP_005251921.1:n.1483+436_1483+439delinsC...
XM_011518437.1:c.*155_*158delinsCTTT XP_011516739.1:n.*155_*158delinsCTTT
XM_011518438.1:c.*155_*158delinsCTTT XP_011516740.1:n.*155_*158delinsCTTT
XM_011518439.1:c.*155_*158delinsCTTT XP_011516741.1:n.*155_*158delinsCTTT
XR_242581.2:n.1816_1819delinsCTTT
XR_242582.2:n.1380+436_1380+439delinsCTTT
XM_005251864.4:c.1483+436_1483+439delinsCTTT XP_005251921.1:n.1483+436_1483+439delinsC...
XM_011518439.2:c.*155_*158delinsCTTT XP_011516741.1:n.*155_*158delinsCTTT
XM_017014565.2:c.1333+436_1333+439delinsCTTT XP_016870054.1:n.1333+436_1333+439delinsC...
XM_017014566.1:c.*155_*158delinsCTTT XP_016870055.1:n.*155_*158delinsCTTT
XR_242581.4:n.1814_1817delinsCTTT
XR_242582.4:n.1378+436_1378+439delinsCTTT
NM_004957.6:c.*155_*158delinsCTTT MANE Select NP_004948.4:n.*155_*158delinsCTTT