Canonical Allele Identifier: CA1845827027

Gene: PIGO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35092525_35092526delinsAC , CM000671.2:g.35092525_35092526delinsAC	GRCh38
NC_000009.11:g.35092522_35092523delinsAC , CM000671.1:g.35092522_35092523delinsAC	GRCh37
NC_000009.10:g.35082522_35082523delinsAC	NCBI36
NG_031990.1:g.9076_9077delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361778.7:c.1344+17_1344+18delinsGT	ENSP00000354678.2:n.1344+17_1344+18delinsGT
ENST00000700254.1:c.1344+17_1344+18delinsGT	ENSP00000514892.1:n.1344+17_1344+18delinsGT
ENST00000700255.1:c.*541_*542delinsGT	ENSP00000514893.1:n.*541_*542delinsGT
ENST00000700256.1:n.1393_1394delinsGT
ENST00000700257.1:c.1361_1362delinsGT	ENSP00000514894.1:p.Gly454=
ENST00000700259.1:c.1344+17_1344+18delinsGT	ENSP00000514895.1:n.1344+17_1344+18delinsGT
ENST00000700260.1:c.1164+17_1164+18delinsGT	ENSP00000514896.1:n.1164+17_1164+18delinsGT
ENST00000700261.1:c.1360+1_1360+2delinsGT	ENSP00000514897.1:n.1360+1_1360+2delinsGT
ENST00000700262.1:c.1344+17_1344+18delinsGT	ENSP00000514898.1:n.1344+17_1344+18delinsGT
ENST00000700263.1:c.1237_1238delinsGT	ENSP00000514899.1:n.1237_1238delinsGT
ENST00000700264.1:c.1361_1362delinsGT	ENSP00000514900.1:p.Gly454=
ENST00000378617.4:c.1361_1362delinsGT MANE Select	ENSP00000367880.3:p.Gly454=
ENST00000298004.9:c.1344+17_1344+18delinsGT	ENSP00000298004.5:n.1344+17_1344+18delinsGT
ENST00000361778.6:c.1344+17_1344+18delinsGT	ENSP00000354678.2:n.1344+17_1344+18delinsGT
ENST00000378617.3:c.1361_1362delinsGT	ENSP00000367880.3:p.Gly454=
ENST00000465745.6:n.2362_2363delinsGT
ENST00000474436.1:n.2819_2820delinsGT
NM_001201484.1:c.1344+17_1344+18delinsGT	NP_001188413.1:n.1344+17_1344+18delinsGT
NM_032634.3:c.1361_1362delinsGT	NP_116023.2:p.Gly454=
NM_152850.3:c.1344+17_1344+18delinsGT	NP_690577.2:n.1344+17_1344+18delinsGT
XM_005251619.2:c.1361_1362delinsGT	XP_005251676.1:p.Gly454=
XM_011518056.1:c.1361_1362delinsGT	XP_011516358.1:p.Gly454=
XR_242515.1:n.1382_1383delinsGT
XM_005251619.3:c.1361_1362delinsGT	XP_005251676.1:p.Gly454=
XM_017015222.2:c.1361_1362delinsGT	XP_016870711.1:p.Gly454=
XM_017015223.1:c.1344+17_1344+18delinsGT	XP_016870712.1:n.1344+17_1344+18delinsGT
XM_017015224.1:c.1344+17_1344+18delinsGT	XP_016870713.1:n.1344+17_1344+18delinsGT
XR_001746390.1:n.1784_1785delinsGT
XR_001746391.2:n.1365+17_1365+18delinsGT
XR_242515.3:n.1382_1383delinsGT
NM_032634.4:c.1361_1362delinsGT MANE Select	NP_116023.2:p.Gly454=
NM_001201484.2:c.1344+17_1344+18delinsGT	NP_001188413.1:n.1344+17_1344+18delinsGT
NM_152850.4:c.1344+17_1344+18delinsGT	NP_690577.2:n.1344+17_1344+18delinsGT