Canonical Allele Identifier: CA373322792

Gene: PIGO

Linked Data

• ClinVar Variation Id: 2146203
• ClinVar RCV Id: RCV003074442
• dbSNP Id: rs1276296360
• gnomAD v2: 9-35093032-G-A
• gnomAD v3: 9-35093035-G-A
• gnomAD v4: 9-35093035-G-A
• MyVariant Identifiers: chr9:g.35093032G>A (hg19) ; chr9:g.35093035G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35093035G>A , CM000671.2:g.35093035G>A	GRCh38
NC_000009.11:g.35093032G>A , CM000671.1:g.35093032G>A	GRCh37
NC_000009.10:g.35083032G>A	NCBI36
NG_031990.1:g.8567C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361778.7:c.1114C>T	ENSP00000354678.2:p.Gln372Ter
ENST00000700254.1:c.1114C>T	ENSP00000514892.1:p.Gln372Ter
ENST00000700255.1:c.*294C>T	ENSP00000514893.1:n.*294C>T
ENST00000700256.1:n.1146C>T
ENST00000700257.1:c.1114C>T	ENSP00000514894.1:p.Gln372Ter
ENST00000700259.1:c.1114C>T	ENSP00000514895.1:p.Gln372Ter
ENST00000700260.1:c.940-268C>T	ENSP00000514896.1:n.940-268C>T
ENST00000700261.1:c.1114C>T	ENSP00000514897.1:p.Gln372Ter
ENST00000700262.1:c.1114C>T	ENSP00000514898.1:p.Gln372Ter
ENST00000700263.1:c.990C>T	ENSP00000514899.1:n.990C>T
ENST00000700264.1:c.1114C>T	ENSP00000514900.1:p.Gln372Ter
ENST00000378617.4:c.1114C>T MANE Select	ENSP00000367880.3:p.Gln372Ter
ENST00000298004.9:c.1114C>T	ENSP00000298004.5:p.Gln372Ter
ENST00000361778.6:c.1114C>T	ENSP00000354678.2:p.Gln372Ter
ENST00000378617.3:c.1114C>T	ENSP00000367880.3:p.Gln372Ter
ENST00000465745.6:n.1853C>T
ENST00000474436.1:n.2310C>T
NM_001201484.1:c.1114C>T	NP_001188413.1:p.Gln372Ter
NM_032634.3:c.1114C>T	NP_116023.2:p.Gln372Ter
NM_152850.3:c.1114C>T	NP_690577.2:p.Gln372Ter
XM_005251619.2:c.1114C>T	XP_005251676.1:p.Gln372Ter
XM_011518056.1:c.1114C>T	XP_011516358.1:p.Gln372Ter
XR_242515.1:n.1135C>T
XM_005251619.3:c.1114C>T	XP_005251676.1:p.Gln372Ter
XM_017015222.2:c.1114C>T	XP_016870711.1:p.Gln372Ter
XM_017015223.1:c.1114C>T	XP_016870712.1:p.Gln372Ter
XM_017015224.1:c.1114C>T	XP_016870713.1:p.Gln372Ter
XR_001746390.1:n.1537C>T
XR_001746391.2:n.1135C>T
XR_242515.3:n.1135C>T
NM_032634.4:c.1114C>T MANE Select	NP_116023.2:p.Gln372Ter
NM_001201484.2:c.1114C>T	NP_001188413.1:p.Gln372Ter
NM_152850.4:c.1114C>T	NP_690577.2:p.Gln372Ter