Canonical Allele Identifier: CA192709641

Gene: PIGO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35091275T>G , CM000671.2:g.35091275T>G	GRCh38
NC_000009.11:g.35091272T>G , CM000671.1:g.35091272T>G	GRCh37
NC_000009.10:g.35081272T>G	NCBI36
NG_031990.1:g.10327A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032634.4:c.2612A>C MANE Select	NP_116023.2:p.His871Pro
ENST00000378617.4:c.2612A>C MANE Select	ENSP00000367880.3:p.His871Pro
NM_001201484.1:c.1361A>C	NP_001188413.1:p.His454Pro
NM_001201484.2:c.1361A>C	NP_001188413.1:p.His454Pro
NM_032634.3:c.2612A>C	NP_116023.2:p.His871Pro
NM_152850.3:c.1361A>C	NP_690577.2:p.His454Pro
NM_152850.4:c.1361A>C	NP_690577.2:p.His454Pro
ENST00000298004.9:c.1361A>C	ENSP00000298004.5:p.His454Pro
ENST00000361778.6:c.1361A>C	ENSP00000354678.2:p.His454Pro
ENST00000361778.7:c.1361A>C	ENSP00000354678.2:p.His454Pro
ENST00000378617.3:c.2612A>C	ENSP00000367880.3:p.His871Pro
ENST00000465745.6:n.3613A>C
ENST00000474436.1:n.4070A>C
ENST00000700254.1:c.1361A>C	ENSP00000514892.1:p.His454Pro
ENST00000700255.1:c.*1792A>C	ENSP00000514893.1:n.*1792A>C
ENST00000700256.1:n.2644A>C
ENST00000700257.1:c.2612A>C	ENSP00000514894.1:p.His871Pro
ENST00000700258.1:n.603A>C
ENST00000700259.1:c.*175A>C	ENSP00000514895.1:n.*175A>C
ENST00000700260.1:c.1181A>C	ENSP00000514896.1:p.His394Pro
ENST00000700261.1:c.1619A>C	ENSP00000514897.1:p.His540Pro
ENST00000700262.1:c.1361A>C	ENSP00000514898.1:p.His454Pro
ENST00000700263.1:c.2488A>C	ENSP00000514899.1:n.2488A>C
ENST00000700264.1:c.2612A>C	ENSP00000514900.1:p.His871Pro
XM_005251619.2:c.2612A>C	XP_005251676.1:p.His871Pro
XM_005251619.3:c.2612A>C	XP_005251676.1:p.His871Pro
XM_011518056.1:c.2612A>C	XP_011516358.1:p.His871Pro
XM_017015222.2:c.2612A>C	XP_016870711.1:p.His871Pro
XM_017015223.1:c.1361A>C	XP_016870712.1:p.His454Pro
XM_017015224.1:c.1361A>C	XP_016870713.1:p.His454Pro
XR_001746390.1:n.3035A>C
XR_001746391.2:n.1382A>C
XR_242515.1:n.2633A>C
XR_242515.3:n.2633A>C