Canonical Allele Identifier: CA2195381213
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966372_90966374delinsCAG , CM000677.2:g.90966372_90966374delinsCAG GRCh38
NC_000015.9:g.91509602_91509604delinsCAG , CM000677.1:g.91509602_91509604delinsCAG GRCh37
NC_000015.8:g.89310606_89310608delinsCAG NCBI36
NG_050647.1:g.33278_33280delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000394249.8:c.*757_*759delinsCTG (PRC1) MANE Select ENSP00000377793.3:n.*757_*759delinsCTG
ENST00000643536.1:c.*4382_*4384delinsCTG ENSP00000494429.1:n.*4382_*4384delinsCTG
ENST00000361188.9:c.*757_*759delinsCTG (PRC1) ENSP00000354679.5:n.*757_*759delinsCTG
ENST00000394249.7:c.*757_*759delinsCTG (PRC1) ENSP00000377793.3:n.*757_*759delinsCTG
ENST00000556972.6:c.404_406delinsCTG (PRC1) ENSP00000456737.1:n.404_406delinsCTG
NM_001267580.1:c.*800_*802delinsCTG (PRC1) NP_001254509.1:n.*800_*802delinsCTG
NM_003981.3:c.*757_*759delinsCTG (PRC1) NP_003972.1:n.*757_*759delinsCTG
NM_199413.2:c.*757_*759delinsCTG (PRC1) NP_955445.1:n.*757_*759delinsCTG
NR_051984.1:n.4_6delinsCAG (PRC1-AS1)
XM_005254987.1:c.*800_*802delinsCTG (PRC1) XP_005255044.1:n.*800_*802delinsCTG
XM_006720759.1:c.*851_*853delinsCTG (PRC1) XP_006720822.1:n.*851_*853delinsCTG
XM_006720760.1:c.*263_*265delinsCTG (PRC1) XP_006720823.1:n.*263_*265delinsCTG
XM_011522187.1:c.*205_*207delinsCTG (PRC1) XP_011520489.1:n.*205_*207delinsCTG
XM_011522188.1:c.*205_*207delinsCTG (PRC1) XP_011520490.1:n.*205_*207delinsCTG
XM_011522189.1:c.*205_*207delinsCTG (PRC1) XP_011520491.1:n.*205_*207delinsCTG
XM_011522190.1:c.*205_*207delinsCTG (PRC1) XP_011520492.1:n.*205_*207delinsCTG
XM_011522192.1:c.*205_*207delinsCTG (PRC1) XP_011520494.1:n.*205_*207delinsCTG
XM_005254987.3:c.*800_*802delinsCTG (PRC1) XP_005255044.1:n.*800_*802delinsCTG
XM_006720759.2:c.*851_*853delinsCTG (PRC1) XP_006720822.1:n.*851_*853delinsCTG
XM_006720760.2:c.*263_*265delinsCTG (PRC1) XP_006720823.1:n.*263_*265delinsCTG
XM_011522187.2:c.*205_*207delinsCTG (PRC1) XP_011520489.1:n.*205_*207delinsCTG
XM_011522188.3:c.*205_*207delinsCTG (PRC1) XP_011520490.1:n.*205_*207delinsCTG
XM_011522189.2:c.*205_*207delinsCTG (PRC1) XP_011520491.1:n.*205_*207delinsCTG
XM_011522191.3:c.*302_*304delinsCTG (PRC1) XP_011520493.1:n.*302_*304delinsCTG
XM_011522192.2:c.*205_*207delinsCTG (PRC1) XP_011520494.1:n.*205_*207delinsCTG
XM_017022712.2:c.*757_*759delinsCTG (PRC1) XP_016878201.1:n.*757_*759delinsCTG
XM_017022713.2:c.*757_*759delinsCTG (PRC1) XP_016878202.1:n.*757_*759delinsCTG
XM_017022715.2:c.*757_*759delinsCTG (PRC1) XP_016878204.1:n.*757_*759delinsCTG
XM_017022716.2:c.*757_*759delinsCTG (PRC1) XP_016878205.1:n.*757_*759delinsCTG
XM_017022717.1:c.*800_*802delinsCTG (PRC1) XP_016878206.1:n.*800_*802delinsCTG
NM_003981.4:c.*757_*759delinsCTG (PRC1) MANE Select NP_003972.2:n.*757_*759delinsCTG
NM_001267580.2:c.*800_*802delinsCTG (PRC1) NP_001254509.2:n.*800_*802delinsCTG
NM_199413.3:c.*757_*759delinsCTG (PRC1) NP_955445.2:n.*757_*759delinsCTG