Canonical Allele Identifier: CA373321752
Gene: PIGO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35092268G>T , CM000671.2:g.35092268G>T GRCh38
NC_000009.11:g.35092265G>T , CM000671.1:g.35092265G>T GRCh37
NC_000009.10:g.35082265G>T NCBI36
NG_031990.1:g.9334C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361778.7:c.1344+275C>A ENSP00000354678.2:n.1344+275C>A
ENST00000700254.1:c.1344+275C>A ENSP00000514892.1:n.1344+275C>A
ENST00000700255.1:c.*799C>A ENSP00000514893.1:n.*799C>A
ENST00000700256.1:n.1651C>A
ENST00000700257.1:c.1619C>A ENSP00000514894.1:p.Ala540Glu
ENST00000700259.1:c.1344+275C>A ENSP00000514895.1:n.1344+275C>A
ENST00000700260.1:c.1164+275C>A ENSP00000514896.1:n.1164+275C>A
ENST00000700261.1:c.1360+259C>A ENSP00000514897.1:n.1360+259C>A
ENST00000700262.1:c.1344+275C>A ENSP00000514898.1:n.1344+275C>A
ENST00000700263.1:c.1495C>A ENSP00000514899.1:n.1495C>A
ENST00000700264.1:c.1619C>A ENSP00000514900.1:p.Ala540Glu
ENST00000378617.4:c.1619C>A MANE Select ENSP00000367880.3:p.Ala540Glu
ENST00000298004.9:c.1344+275C>A ENSP00000298004.5:n.1344+275C>A
ENST00000361778.6:c.1344+275C>A ENSP00000354678.2:n.1344+275C>A
ENST00000378617.3:c.1619C>A ENSP00000367880.3:p.Ala540Glu
ENST00000465745.6:n.2620C>A
ENST00000474436.1:n.3077C>A
NM_001201484.1:c.1344+275C>A NP_001188413.1:n.1344+275C>A
NM_032634.3:c.1619C>A NP_116023.2:p.Ala540Glu
NM_152850.3:c.1344+275C>A NP_690577.2:n.1344+275C>A
XM_005251619.2:c.1619C>A XP_005251676.1:p.Ala540Glu
XM_011518056.1:c.1619C>A XP_011516358.1:p.Ala540Glu
XR_242515.1:n.1640C>A
XM_005251619.3:c.1619C>A XP_005251676.1:p.Ala540Glu
XM_017015222.2:c.1619C>A XP_016870711.1:p.Ala540Glu
XM_017015223.1:c.1344+275C>A XP_016870712.1:n.1344+275C>A
XM_017015224.1:c.1344+275C>A XP_016870713.1:n.1344+275C>A
XR_001746390.1:n.2042C>A
XR_001746391.2:n.1365+275C>A
XR_242515.3:n.1640C>A
NM_032634.4:c.1619C>A MANE Select NP_116023.2:p.Ala540Glu
NM_001201484.2:c.1344+275C>A NP_001188413.1:n.1344+275C>A
NM_152850.4:c.1344+275C>A NP_690577.2:n.1344+275C>A