Canonical Allele Identifier: CA1123180700
Gene: PIGO HGNC NCBI

Linked Data

dbSNP Id: rs1829563094
gnomAD v4: 9-35094161-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35094161A>G , CM000671.2:g.35094161A>G GRCh38
NC_000009.11:g.35094158A>G , CM000671.1:g.35094158A>G GRCh37
NC_000009.10:g.35084158A>G NCBI36
NG_031990.1:g.7441T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361778.7:c.655+55T>C ENSP00000354678.2:n.655+55T>C
ENST00000700254.1:c.655+55T>C ENSP00000514892.1:n.655+55T>C
ENST00000700255.1:c.655+55T>C ENSP00000514893.1:n.655+55T>C
ENST00000700256.1:n.687+55T>C
ENST00000700257.1:c.655+55T>C ENSP00000514894.1:n.655+55T>C
ENST00000700259.1:c.655+55T>C ENSP00000514895.1:n.655+55T>C
ENST00000700260.1:c.655+55T>C ENSP00000514896.1:n.655+55T>C
ENST00000700261.1:c.655+55T>C ENSP00000514897.1:n.655+55T>C
ENST00000700262.1:c.655+55T>C ENSP00000514898.1:n.655+55T>C
ENST00000700263.1:c.655+55T>C ENSP00000514899.1:n.655+55T>C
ENST00000700264.1:c.655+55T>C ENSP00000514900.1:n.655+55T>C
ENST00000378617.4:c.655+55T>C MANE Select ENSP00000367880.3:n.655+55T>C
ENST00000298004.9:c.655+55T>C ENSP00000298004.5:n.655+55T>C
ENST00000361778.6:c.655+55T>C ENSP00000354678.2:n.655+55T>C
ENST00000378617.3:c.655+55T>C ENSP00000367880.3:n.655+55T>C
ENST00000465745.6:n.727T>C
ENST00000474436.1:n.1640+55T>C
NM_001201484.1:c.655+55T>C NP_001188413.1:n.655+55T>C
NM_032634.3:c.655+55T>C NP_116023.2:n.655+55T>C
NM_152850.3:c.655+55T>C NP_690577.2:n.655+55T>C
XM_005251619.2:c.655+55T>C XP_005251676.1:n.655+55T>C
XM_011518056.1:c.655+55T>C XP_011516358.1:n.655+55T>C
XR_242515.1:n.676+55T>C
XM_005251619.3:c.655+55T>C XP_005251676.1:n.655+55T>C
XM_017015222.2:c.655+55T>C XP_016870711.1:n.655+55T>C
XM_017015223.1:c.655+55T>C XP_016870712.1:n.655+55T>C
XM_017015224.1:c.655+55T>C XP_016870713.1:n.655+55T>C
XR_001746390.1:n.1078+55T>C
XR_001746391.2:n.676+55T>C
XR_242515.3:n.676+55T>C
NM_032634.4:c.655+55T>C MANE Select NP_116023.2:n.655+55T>C
NM_001201484.2:c.655+55T>C NP_001188413.1:n.655+55T>C
NM_152850.4:c.655+55T>C NP_690577.2:n.655+55T>C