Canonical Allele Identifier: CA2840389769
Gene: PIGO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35092414dup , CM000671.2:g.35092414dup GRCh38
NC_000009.11:g.35092411dup , CM000671.1:g.35092411dup GRCh37
NC_000009.10:g.35082411dup NCBI36
NG_031990.1:g.9189dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361778.7:c.1344+130dup ENSP00000354678.2:n.1344+130dup
ENST00000700254.1:c.1344+130dup ENSP00000514892.1:n.1344+130dup
ENST00000700255.1:c.*654dup ENSP00000514893.1:n.*654dup
ENST00000700256.1:n.1506dup
ENST00000700257.1:c.1474dup ENSP00000514894.1:p.Val492GlyfsTer14
ENST00000700259.1:c.1344+130dup ENSP00000514895.1:n.1344+130dup
ENST00000700260.1:c.1164+130dup ENSP00000514896.1:n.1164+130dup
ENST00000700261.1:c.1360+114dup ENSP00000514897.1:n.1360+114dup
ENST00000700262.1:c.1344+130dup ENSP00000514898.1:n.1344+130dup
ENST00000700263.1:c.1350dup ENSP00000514899.1:n.1350dup
ENST00000700264.1:c.1474dup ENSP00000514900.1:p.Val492GlyfsTer14
ENST00000378617.4:c.1474dup MANE Select ENSP00000367880.3:p.Val492GlyfsTer14
ENST00000298004.9:c.1344+130dup ENSP00000298004.5:n.1344+130dup
ENST00000361778.6:c.1344+130dup ENSP00000354678.2:n.1344+130dup
ENST00000378617.3:c.1474dup ENSP00000367880.3:p.Val492GlyfsTer14
ENST00000465745.6:n.2475dup
ENST00000474436.1:n.2932dup
NM_001201484.1:c.1344+130dup NP_001188413.1:n.1344+130dup
NM_032634.3:c.1474dup NP_116023.2:p.Val492GlyfsTer14
NM_152850.3:c.1344+130dup NP_690577.2:n.1344+130dup
XM_005251619.2:c.1474dup XP_005251676.1:p.Val492GlyfsTer14
XM_011518056.1:c.1474dup XP_011516358.1:p.Val492GlyfsTer14
XR_242515.1:n.1495dup
XM_005251619.3:c.1474dup XP_005251676.1:p.Val492GlyfsTer14
XM_017015222.2:c.1474dup XP_016870711.1:p.Val492GlyfsTer14
XM_017015223.1:c.1344+130dup XP_016870712.1:n.1344+130dup
XM_017015224.1:c.1344+130dup XP_016870713.1:n.1344+130dup
XR_001746390.1:n.1897dup
XR_001746391.2:n.1365+130dup
XR_242515.3:n.1495dup
NM_032634.4:c.1474dup MANE Select NP_116023.2:p.Val492GlyfsTer14
NM_001201484.2:c.1344+130dup NP_001188413.1:n.1344+130dup
NM_152850.4:c.1344+130dup NP_690577.2:n.1344+130dup