Canonical Allele Identifier: CA1123180194
Gene: PIGO HGNC NCBI

Linked Data

dbSNP Id: rs986560200
gnomAD v3: 9-35092917-G-C
gnomAD v4: 9-35092917-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35092917G>C , CM000671.2:g.35092917G>C GRCh38
NC_000009.11:g.35092914G>C , CM000671.1:g.35092914G>C GRCh37
NC_000009.10:g.35082914G>C NCBI36
NG_031990.1:g.8685C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361778.7:c.1119+113C>G ENSP00000354678.2:n.1119+113C>G
ENST00000700254.1:c.1119+113C>G ENSP00000514892.1:n.1119+113C>G
ENST00000700255.1:c.*299+113C>G ENSP00000514893.1:n.*299+113C>G
ENST00000700256.1:n.1151+113C>G
ENST00000700257.1:c.1119+113C>G ENSP00000514894.1:n.1119+113C>G
ENST00000700259.1:c.1119+113C>G ENSP00000514895.1:n.1119+113C>G
ENST00000700260.1:c.940-150C>G ENSP00000514896.1:n.940-150C>G
ENST00000700261.1:c.1119+113C>G ENSP00000514897.1:n.1119+113C>G
ENST00000700262.1:c.1119+113C>G ENSP00000514898.1:n.1119+113C>G
ENST00000700263.1:c.995+113C>G ENSP00000514899.1:n.995+113C>G
ENST00000700264.1:c.1119+113C>G ENSP00000514900.1:n.1119+113C>G
ENST00000378617.4:c.1119+113C>G MANE Select ENSP00000367880.3:n.1119+113C>G
ENST00000298004.9:c.1119+113C>G ENSP00000298004.5:n.1119+113C>G
ENST00000361778.6:c.1119+113C>G ENSP00000354678.2:n.1119+113C>G
ENST00000378617.3:c.1119+113C>G ENSP00000367880.3:n.1119+113C>G
ENST00000465745.6:n.1971C>G
ENST00000474436.1:n.2428C>G
NM_001201484.1:c.1119+113C>G NP_001188413.1:n.1119+113C>G
NM_032634.3:c.1119+113C>G NP_116023.2:n.1119+113C>G
NM_152850.3:c.1119+113C>G NP_690577.2:n.1119+113C>G
XM_005251619.2:c.1119+113C>G XP_005251676.1:n.1119+113C>G
XM_011518056.1:c.1119+113C>G XP_011516358.1:n.1119+113C>G
XR_242515.1:n.1140+113C>G
XM_005251619.3:c.1119+113C>G XP_005251676.1:n.1119+113C>G
XM_017015222.2:c.1119+113C>G XP_016870711.1:n.1119+113C>G
XM_017015223.1:c.1119+113C>G XP_016870712.1:n.1119+113C>G
XM_017015224.1:c.1119+113C>G XP_016870713.1:n.1119+113C>G
XR_001746390.1:n.1542+113C>G
XR_001746391.2:n.1140+113C>G
XR_242515.3:n.1140+113C>G
NM_032634.4:c.1119+113C>G MANE Select NP_116023.2:n.1119+113C>G
NM_001201484.2:c.1119+113C>G NP_001188413.1:n.1119+113C>G
NM_152850.4:c.1119+113C>G NP_690577.2:n.1119+113C>G