Canonical Allele Identifier: CA1845826991

Gene: PIGO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35092437_35092442delinsGGAGTA , CM000671.2:g.35092437_35092442delinsGGAGTA	GRCh38
NC_000009.11:g.35092434_35092439delinsGGAGTA , CM000671.1:g.35092434_35092439delinsGGAGTA	GRCh37
NC_000009.10:g.35082434_35082439delinsGGAGTA	NCBI36
NG_031990.1:g.9160_9165delinsTACTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000361778.7:c.1344+101_1344+106delinsTACTCC	ENSP00000354678.2:n.1344+101_1344+106deli...
ENST00000700254.1:c.1344+101_1344+106delinsTACTCC	ENSP00000514892.1:n.1344+101_1344+106deli...
ENST00000700255.1:c.*625_*630delinsTACTCC	ENSP00000514893.1:n.*625_*630delinsTACTCC...
ENST00000700256.1:n.1477_1482delinsTACTCC
ENST00000700257.1:c.1445_1450delinsTACTCC	ENSP00000514894.1:p.Leu482=
ENST00000700259.1:c.1344+101_1344+106delinsTACTCC	ENSP00000514895.1:n.1344+101_1344+106deli...
ENST00000700260.1:c.1164+101_1164+106delinsTACTCC	ENSP00000514896.1:n.1164+101_1164+106deli...
ENST00000700261.1:c.1360+85_1360+90delinsTACTCC	ENSP00000514897.1:n.1360+85_1360+90delins...
ENST00000700262.1:c.1344+101_1344+106delinsTACTCC	ENSP00000514898.1:n.1344+101_1344+106deli...
ENST00000700263.1:c.1321_1326delinsTACTCC	ENSP00000514899.1:n.1321_1326delinsTACTCC...
ENST00000700264.1:c.1445_1450delinsTACTCC	ENSP00000514900.1:p.Leu482=
ENST00000378617.4:c.1445_1450delinsTACTCC MANE Select	ENSP00000367880.3:p.Leu482=
ENST00000298004.9:c.1344+101_1344+106delinsTACTCC	ENSP00000298004.5:n.1344+101_1344+106deli...
ENST00000361778.6:c.1344+101_1344+106delinsTACTCC	ENSP00000354678.2:n.1344+101_1344+106deli...
ENST00000378617.3:c.1445_1450delinsTACTCC	ENSP00000367880.3:p.Leu482=
ENST00000465745.6:n.2446_2451delinsTACTCC
ENST00000474436.1:n.2903_2908delinsTACTCC
NM_001201484.1:c.1344+101_1344+106delinsTACTCC	NP_001188413.1:n.1344+101_1344+106delinsT...
NM_032634.3:c.1445_1450delinsTACTCC	NP_116023.2:p.Leu482=
NM_152850.3:c.1344+101_1344+106delinsTACTCC	NP_690577.2:n.1344+101_1344+106delinsTACT...
XM_005251619.2:c.1445_1450delinsTACTCC	XP_005251676.1:p.Leu482=
XM_011518056.1:c.1445_1450delinsTACTCC	XP_011516358.1:p.Leu482=
XR_242515.1:n.1466_1471delinsTACTCC
XM_005251619.3:c.1445_1450delinsTACTCC	XP_005251676.1:p.Leu482=
XM_017015222.2:c.1445_1450delinsTACTCC	XP_016870711.1:p.Leu482=
XM_017015223.1:c.1344+101_1344+106delinsTACTCC	XP_016870712.1:n.1344+101_1344+106delinsT...
XM_017015224.1:c.1344+101_1344+106delinsTACTCC	XP_016870713.1:n.1344+101_1344+106delinsT...
XR_001746390.1:n.1868_1873delinsTACTCC
XR_001746391.2:n.1365+101_1365+106delinsTACTCC
XR_242515.3:n.1466_1471delinsTACTCC
NM_032634.4:c.1445_1450delinsTACTCC MANE Select	NP_116023.2:p.Leu482=
NM_001201484.2:c.1344+101_1344+106delinsTACTCC	NP_001188413.1:n.1344+101_1344+106delinsT...
NM_152850.4:c.1344+101_1344+106delinsTACTCC	NP_690577.2:n.1344+101_1344+106delinsTACT...