Canonical Allele Identifier: CA1845826995
Gene: PIGO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35092445G= , CM000671.2:g.35092445G= GRCh38
NC_000009.11:g.35092442G= , CM000671.1:g.35092442G= GRCh37
NC_000009.10:g.35082442G= NCBI36
NG_031990.1:g.9157C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361778.7:c.1344+98C= ENSP00000354678.2:n.1344+98C=
ENST00000700254.1:c.1344+98C= ENSP00000514892.1:n.1344+98C=
ENST00000700255.1:c.*622C= ENSP00000514893.1:n.*622C=
ENST00000700256.1:n.1474C=
ENST00000700257.1:c.1442C= ENSP00000514894.1:p.Pro481=
ENST00000700259.1:c.1344+98C= ENSP00000514895.1:n.1344+98C=
ENST00000700260.1:c.1164+98C= ENSP00000514896.1:n.1164+98C=
ENST00000700261.1:c.1360+82C= ENSP00000514897.1:n.1360+82C=
ENST00000700262.1:c.1344+98C= ENSP00000514898.1:n.1344+98C=
ENST00000700263.1:c.1318C= ENSP00000514899.1:n.1318C=
ENST00000700264.1:c.1442C= ENSP00000514900.1:p.Pro481=
ENST00000378617.4:c.1442C= MANE Select ENSP00000367880.3:p.Pro481=
ENST00000298004.9:c.1344+98C= ENSP00000298004.5:n.1344+98C=
ENST00000361778.6:c.1344+98C= ENSP00000354678.2:n.1344+98C=
ENST00000378617.3:c.1442C= ENSP00000367880.3:p.Pro481=
ENST00000465745.6:n.2443C=
ENST00000474436.1:n.2900C=
NM_001201484.1:c.1344+98C= NP_001188413.1:n.1344+98C=
NM_032634.3:c.1442C= NP_116023.2:p.Pro481=
NM_152850.3:c.1344+98C= NP_690577.2:n.1344+98C=
XM_005251619.2:c.1442C= XP_005251676.1:p.Pro481=
XM_011518056.1:c.1442C= XP_011516358.1:p.Pro481=
XR_242515.1:n.1463C=
XM_005251619.3:c.1442C= XP_005251676.1:p.Pro481=
XM_017015222.2:c.1442C= XP_016870711.1:p.Pro481=
XM_017015223.1:c.1344+98C= XP_016870712.1:n.1344+98C=
XM_017015224.1:c.1344+98C= XP_016870713.1:n.1344+98C=
XR_001746390.1:n.1865C=
XR_001746391.2:n.1365+98C=
XR_242515.3:n.1463C=
NM_032634.4:c.1442C= MANE Select NP_116023.2:p.Pro481=
NM_001201484.2:c.1344+98C= NP_001188413.1:n.1344+98C=
NM_152850.4:c.1344+98C= NP_690577.2:n.1344+98C=