Canonical Allele Identifier: CA717053031

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs1411919493
• gnomAD v3: 15-90966372-CAG-C
• gnomAD v4: 15-90966372-CAG-C
• MyVariant Identifiers: chr15:g.91509603_91509604del (hg19) ; chr15:g.90966373_90966374del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966374_90966375del , CM000677.2:g.90966374_90966375del	GRCh38
NC_000015.9:g.91509604_91509605del , CM000677.1:g.91509604_91509605del	GRCh37
NC_000015.8:g.89310608_89310609del	NCBI36
NG_050647.1:g.33278_33279del

Transcript Alleles

HGVS	Amino-acid change
ENST00000394249.8:c.*757_*758del (PRC1) MANE Select	ENSP00000377793.3:n.*757_*758del
ENST00000643536.1:c.*4382_*4383del	ENSP00000494429.1:n.*4382_*4383del
ENST00000361188.9:c.*757_*758del (PRC1)	ENSP00000354679.5:n.*757_*758del
ENST00000394249.7:c.*757_*758del (PRC1)	ENSP00000377793.3:n.*757_*758del
ENST00000556972.6:c.404_405del (PRC1)	ENSP00000456737.1:n.404_405del
NM_001267580.1:c.*800_*801del (PRC1)	NP_001254509.1:n.*800_*801del
NM_003981.3:c.*757_*758del (PRC1)	NP_003972.1:n.*757_*758del
NM_199413.2:c.*757_*758del (PRC1)	NP_955445.1:n.*757_*758del
NR_051984.1:n.6_7del (PRC1-AS1)
XM_005254987.1:c.*800_*801del (PRC1)	XP_005255044.1:n.*800_*801del
XM_006720759.1:c.*851_*852del (PRC1)	XP_006720822.1:n.*851_*852del
XM_006720760.1:c.*263_*264del (PRC1)	XP_006720823.1:n.*263_*264del
XM_011522187.1:c.*205_*206del (PRC1)	XP_011520489.1:n.*205_*206del
XM_011522188.1:c.*205_*206del (PRC1)	XP_011520490.1:n.*205_*206del
XM_011522189.1:c.*205_*206del (PRC1)	XP_011520491.1:n.*205_*206del
XM_011522190.1:c.*205_*206del (PRC1)	XP_011520492.1:n.*205_*206del
XM_011522192.1:c.*205_*206del (PRC1)	XP_011520494.1:n.*205_*206del
XM_005254987.3:c.*800_*801del (PRC1)	XP_005255044.1:n.*800_*801del
XM_006720759.2:c.*851_*852del (PRC1)	XP_006720822.1:n.*851_*852del
XM_006720760.2:c.*263_*264del (PRC1)	XP_006720823.1:n.*263_*264del
XM_011522187.2:c.*205_*206del (PRC1)	XP_011520489.1:n.*205_*206del
XM_011522188.3:c.*205_*206del (PRC1)	XP_011520490.1:n.*205_*206del
XM_011522189.2:c.*205_*206del (PRC1)	XP_011520491.1:n.*205_*206del
XM_011522191.3:c.*302_*303del (PRC1)	XP_011520493.1:n.*302_*303del
XM_011522192.2:c.*205_*206del (PRC1)	XP_011520494.1:n.*205_*206del
XM_017022712.2:c.*757_*758del (PRC1)	XP_016878201.1:n.*757_*758del
XM_017022713.2:c.*757_*758del (PRC1)	XP_016878202.1:n.*757_*758del
XM_017022715.2:c.*757_*758del (PRC1)	XP_016878204.1:n.*757_*758del
XM_017022716.2:c.*757_*758del (PRC1)	XP_016878205.1:n.*757_*758del
XM_017022717.1:c.*800_*801del (PRC1)	XP_016878206.1:n.*800_*801del
NM_003981.4:c.*757_*758del (PRC1) MANE Select	NP_003972.2:n.*757_*758del
NM_001267580.2:c.*800_*801del (PRC1)	NP_001254509.2:n.*800_*801del
NM_199413.3:c.*757_*758del (PRC1)	NP_955445.2:n.*757_*758del