Canonical Allele Identifier: CA1845871263

Gene: PIGO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35092337_35092338delinsGC , CM000671.2:g.35092337_35092338delinsGC	GRCh38
NC_000009.11:g.35092334_35092335delinsGC , CM000671.1:g.35092334_35092335delinsGC	GRCh37
NC_000009.10:g.35082334_35082335delinsGC	NCBI36
NG_031990.1:g.9264_9265delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361778.7:c.1344+205_1344+206delinsGC	ENSP00000354678.2:n.1344+205_1344+206delinsGC
ENST00000700254.1:c.1344+205_1344+206delinsGC	ENSP00000514892.1:n.1344+205_1344+206delinsGC
ENST00000700255.1:c.*729_*730delinsGC	ENSP00000514893.1:n.*729_*730delinsGC
ENST00000700256.1:n.1581_1582delinsGC
ENST00000700257.1:c.1549_1550delinsGC	ENSP00000514894.1:p.Ala517=
ENST00000700259.1:c.1344+205_1344+206delinsGC	ENSP00000514895.1:n.1344+205_1344+206delinsGC
ENST00000700260.1:c.1164+205_1164+206delinsGC	ENSP00000514896.1:n.1164+205_1164+206delinsGC
ENST00000700261.1:c.1360+189_1360+190delinsGC	ENSP00000514897.1:n.1360+189_1360+190delinsGC
ENST00000700262.1:c.1344+205_1344+206delinsGC	ENSP00000514898.1:n.1344+205_1344+206delinsGC
ENST00000700263.1:c.1425_1426delinsGC	ENSP00000514899.1:n.1425_1426delinsGC
ENST00000700264.1:c.1549_1550delinsGC	ENSP00000514900.1:p.Ala517=
ENST00000378617.4:c.1549_1550delinsGC MANE Select	ENSP00000367880.3:p.Ala517=
ENST00000298004.9:c.1344+205_1344+206delinsGC	ENSP00000298004.5:n.1344+205_1344+206delinsGC
ENST00000361778.6:c.1344+205_1344+206delinsGC	ENSP00000354678.2:n.1344+205_1344+206delinsGC
ENST00000378617.3:c.1549_1550delinsGC	ENSP00000367880.3:p.Ala517=
ENST00000465745.6:n.2550_2551delinsGC
ENST00000474436.1:n.3007_3008delinsGC
NM_001201484.1:c.1344+205_1344+206delinsGC	NP_001188413.1:n.1344+205_1344+206delinsGC
NM_032634.3:c.1549_1550delinsGC	NP_116023.2:p.Ala517=
NM_152850.3:c.1344+205_1344+206delinsGC	NP_690577.2:n.1344+205_1344+206delinsGC
XM_005251619.2:c.1549_1550delinsGC	XP_005251676.1:p.Ala517=
XM_011518056.1:c.1549_1550delinsGC	XP_011516358.1:p.Ala517=
XR_242515.1:n.1570_1571delinsGC
XM_005251619.3:c.1549_1550delinsGC	XP_005251676.1:p.Ala517=
XM_017015222.2:c.1549_1550delinsGC	XP_016870711.1:p.Ala517=
XM_017015223.1:c.1344+205_1344+206delinsGC	XP_016870712.1:n.1344+205_1344+206delinsGC
XM_017015224.1:c.1344+205_1344+206delinsGC	XP_016870713.1:n.1344+205_1344+206delinsGC
XR_001746390.1:n.1972_1973delinsGC
XR_001746391.2:n.1365+205_1365+206delinsGC
XR_242515.3:n.1570_1571delinsGC
NM_032634.4:c.1549_1550delinsGC MANE Select	NP_116023.2:p.Ala517=
NM_001201484.2:c.1344+205_1344+206delinsGC	NP_001188413.1:n.1344+205_1344+206delinsGC
NM_152850.4:c.1344+205_1344+206delinsGC	NP_690577.2:n.1344+205_1344+206delinsGC