Canonical Allele Identifier: CA1845871214

Gene: PIGO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35092305_35092337delinsTCCACAGAAAAGGGAGGAATGAGCTCACTGCAG , CM000671.2:g.35092305_35092337delinsTCCACAGAAAAGGGAGGAATGAGCTCACTGCAG	GRCh38
NC_000009.11:g.35092302_35092334delinsTCCACAGAAAAGGGAGGAATGAGCTCACTGCAG , CM000671.1:g.35092302_35092334delinsTCCACAGAAAAGGGAGGAATGAGCTCACTGCAG	GRCh37
NC_000009.10:g.35082302_35082334delinsTCCACAGAAAAGGGAGGAATGAGCTCACTGCAG	NCBI36
NG_031990.1:g.9265_9297delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361778.7:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000354678.2:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCC...
ENST00000700254.1:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000514892.1:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCC...
ENST00000700255.1:c.*730_*762delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000514893.1:n.*730_*762delinsCTGCAGTGAGCTCATTCCTCCCTTTT...
ENST00000700256.1:n.1582_1614delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA
ENST00000700257.1:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000514894.1:p.Ala517=
ENST00000700259.1:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000514895.1:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCC...
ENST00000700260.1:c.1164+206_1164+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000514896.1:n.1164+206_1164+238delinsCTGCAGTGAGCTCATTCC...
ENST00000700261.1:c.1360+190_1360+222delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000514897.1:n.1360+190_1360+222delinsCTGCAGTGAGCTCATTCC...
ENST00000700262.1:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000514898.1:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCC...
ENST00000700263.1:c.1426_1458delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000514899.1:n.1426_1458delinsCTGCAGTGAGCTCATTCCTCCCTTTT...
ENST00000700264.1:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000514900.1:p.Ala517=
ENST00000378617.4:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA MANE Select	ENSP00000367880.3:p.Ala517=
ENST00000298004.9:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000298004.5:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCC...
ENST00000361778.6:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000354678.2:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCC...
ENST00000378617.3:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	ENSP00000367880.3:p.Ala517=
ENST00000465745.6:n.2551_2583delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA
ENST00000474436.1:n.3008_3040delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA
NM_001201484.1:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	NP_001188413.1:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCC...
NM_032634.3:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	NP_116023.2:p.Ala517=
NM_152850.3:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	NP_690577.2:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTT...
XM_005251619.2:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	XP_005251676.1:p.Ala517=
XM_011518056.1:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	XP_011516358.1:p.Ala517=
XR_242515.1:n.1571_1603delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA
XM_005251619.3:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	XP_005251676.1:p.Ala517=
XM_017015222.2:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	XP_016870711.1:p.Ala517=
XM_017015223.1:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	XP_016870712.1:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCC...
XM_017015224.1:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	XP_016870713.1:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCC...
XR_001746390.1:n.1973_2005delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA
XR_001746391.2:n.1365+206_1365+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA
XR_242515.3:n.1571_1603delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA
NM_032634.4:c.1550_1582delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA MANE Select	NP_116023.2:p.Ala517=
NM_001201484.2:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	NP_001188413.1:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCC...
NM_152850.4:c.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTTTTCTGTGGA	NP_690577.2:n.1344+206_1344+238delinsCTGCAGTGAGCTCATTCCTCCCTT...