Canonical Allele Identifier: CA373322098

Gene: PIGO

Linked Data

• MyVariant Identifiers: chr9:g.35092439A>C (hg19) ; chr9:g.35092442A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35092442A>C , CM000671.2:g.35092442A>C	GRCh38
NC_000009.11:g.35092439A>C , CM000671.1:g.35092439A>C	GRCh37
NC_000009.10:g.35082439A>C	NCBI36
NG_031990.1:g.9160T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361778.7:c.1344+101T>G	ENSP00000354678.2:n.1344+101T>G
ENST00000700254.1:c.1344+101T>G	ENSP00000514892.1:n.1344+101T>G
ENST00000700255.1:c.*625T>G	ENSP00000514893.1:n.*625T>G
ENST00000700256.1:n.1477T>G
ENST00000700257.1:c.1445T>G	ENSP00000514894.1:p.Leu482Arg
ENST00000700259.1:c.1344+101T>G	ENSP00000514895.1:n.1344+101T>G
ENST00000700260.1:c.1164+101T>G	ENSP00000514896.1:n.1164+101T>G
ENST00000700261.1:c.1360+85T>G	ENSP00000514897.1:n.1360+85T>G
ENST00000700262.1:c.1344+101T>G	ENSP00000514898.1:n.1344+101T>G
ENST00000700263.1:c.1321T>G	ENSP00000514899.1:n.1321T>G
ENST00000700264.1:c.1445T>G	ENSP00000514900.1:p.Leu482Arg
ENST00000378617.4:c.1445T>G MANE Select	ENSP00000367880.3:p.Leu482Arg
ENST00000298004.9:c.1344+101T>G	ENSP00000298004.5:n.1344+101T>G
ENST00000361778.6:c.1344+101T>G	ENSP00000354678.2:n.1344+101T>G
ENST00000378617.3:c.1445T>G	ENSP00000367880.3:p.Leu482Arg
ENST00000465745.6:n.2446T>G
ENST00000474436.1:n.2903T>G
NM_001201484.1:c.1344+101T>G	NP_001188413.1:n.1344+101T>G
NM_032634.3:c.1445T>G	NP_116023.2:p.Leu482Arg
NM_152850.3:c.1344+101T>G	NP_690577.2:n.1344+101T>G
XM_005251619.2:c.1445T>G	XP_005251676.1:p.Leu482Arg
XM_011518056.1:c.1445T>G	XP_011516358.1:p.Leu482Arg
XR_242515.1:n.1466T>G
XM_005251619.3:c.1445T>G	XP_005251676.1:p.Leu482Arg
XM_017015222.2:c.1445T>G	XP_016870711.1:p.Leu482Arg
XM_017015223.1:c.1344+101T>G	XP_016870712.1:n.1344+101T>G
XM_017015224.1:c.1344+101T>G	XP_016870713.1:n.1344+101T>G
XR_001746390.1:n.1868T>G
XR_001746391.2:n.1365+101T>G
XR_242515.3:n.1466T>G
NM_032634.4:c.1445T>G MANE Select	NP_116023.2:p.Leu482Arg
NM_001201484.2:c.1344+101T>G	NP_001188413.1:n.1344+101T>G
NM_152850.4:c.1344+101T>G	NP_690577.2:n.1344+101T>G