Canonical Allele Identifier: CA2970677993

Gene: PIGO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35094146dup , CM000671.2:g.35094146dup	GRCh38
NC_000009.11:g.35094143dup , CM000671.1:g.35094143dup	GRCh37
NC_000009.10:g.35084143dup	NCBI36
NG_031990.1:g.7456dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361778.7:c.655+70dup	ENSP00000354678.2:n.655+70dup
ENST00000700254.1:c.655+70dup	ENSP00000514892.1:n.655+70dup
ENST00000700255.1:c.655+70dup	ENSP00000514893.1:n.655+70dup
ENST00000700256.1:n.687+70dup
ENST00000700257.1:c.655+70dup	ENSP00000514894.1:n.655+70dup
ENST00000700259.1:c.655+70dup	ENSP00000514895.1:n.655+70dup
ENST00000700260.1:c.655+70dup	ENSP00000514896.1:n.655+70dup
ENST00000700261.1:c.655+70dup	ENSP00000514897.1:n.655+70dup
ENST00000700262.1:c.655+70dup	ENSP00000514898.1:n.655+70dup
ENST00000700263.1:c.655+70dup	ENSP00000514899.1:n.655+70dup
ENST00000700264.1:c.655+70dup	ENSP00000514900.1:n.655+70dup
ENST00000378617.4:c.655+70dup MANE Select	ENSP00000367880.3:n.655+70dup
ENST00000298004.9:c.655+70dup	ENSP00000298004.5:n.655+70dup
ENST00000361778.6:c.655+70dup	ENSP00000354678.2:n.655+70dup
ENST00000378617.3:c.655+70dup	ENSP00000367880.3:n.655+70dup
ENST00000465745.6:n.742dup
ENST00000474436.1:n.1640+70dup
NM_001201484.1:c.655+70dup	NP_001188413.1:n.655+70dup
NM_032634.3:c.655+70dup	NP_116023.2:n.655+70dup
NM_152850.3:c.655+70dup	NP_690577.2:n.655+70dup
XM_005251619.2:c.655+70dup	XP_005251676.1:n.655+70dup
XM_011518056.1:c.655+70dup	XP_011516358.1:n.655+70dup
XR_242515.1:n.676+70dup
XM_005251619.3:c.655+70dup	XP_005251676.1:n.655+70dup
XM_017015222.2:c.655+70dup	XP_016870711.1:n.655+70dup
XM_017015223.1:c.655+70dup	XP_016870712.1:n.655+70dup
XM_017015224.1:c.655+70dup	XP_016870713.1:n.655+70dup
XR_001746390.1:n.1078+70dup
XR_001746391.2:n.676+70dup
XR_242515.3:n.676+70dup
NM_032634.4:c.655+70dup MANE Select	NP_116023.2:n.655+70dup
NM_001201484.2:c.655+70dup	NP_001188413.1:n.655+70dup
NM_152850.4:c.655+70dup	NP_690577.2:n.655+70dup