Canonical Allele Identifier: CA15838513
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2290203

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90968837G>A , CM000677.2:g.90968837G>A GRCh38
NC_000015.9:g.91512067G>A , CM000677.1:g.91512067G>A GRCh37
NC_000015.8:g.89313071G>A NCBI36
NG_050647.1:g.30815C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394249.8:c.1791+242C>T (PRC1) MANE Select ENSP00000377793.3:n.1791+242C>T
ENST00000643536.1:c.*1919C>T ENSP00000494429.1:n.*1919C>T
ENST00000361188.9:c.1749+610C>T (PRC1) ENSP00000354679.5:n.1749+610C>T
ENST00000394249.7:c.1791+242C>T (PRC1) ENSP00000377793.3:n.1791+242C>T
ENST00000442656.6:c.1549+687C>T (PRC1) ENSP00000409549.2:n.1549+687C>T
ENST00000555455.5:c.641+242C>T (PRC1)
ENST00000556972.6:c.124+687C>T (PRC1) ENSP00000456737.1:n.124+687C>T
ENST00000560423.5:c.216+242C>T (PRC1)
NM_001267580.1:c.1549+687C>T (PRC1) NP_001254509.1:n.1549+687C>T
NM_003981.3:c.1791+242C>T (PRC1) NP_003972.1:n.1791+242C>T
NM_199413.2:c.1749+610C>T (PRC1) NP_955445.1:n.1749+610C>T
NR_051984.1:n.310+2159G>A (PRC1-AS1)
XM_005254987.1:c.1672+687C>T (PRC1) XP_005255044.1:n.1672+687C>T
XM_006720759.1:c.*22+242C>T (PRC1) XP_006720822.1:n.*22+242C>T
XM_006720760.1:c.1672+687C>T (PRC1) XP_006720823.1:n.1672+687C>T
XM_011522187.1:c.1791+242C>T (PRC1) XP_011520489.1:n.1791+242C>T
XM_011522188.1:c.1749+610C>T (PRC1) XP_011520490.1:n.1749+610C>T
XM_011522189.1:c.1680+242C>T (PRC1) XP_011520491.1:n.1680+242C>T
XM_011522190.1:c.1620+242C>T (PRC1) XP_011520492.1:n.1620+242C>T
XM_011522191.1:c.*22+242C>T (PRC1) XP_011520493.1:n.*22+242C>T
XM_011522192.1:c.1470+242C>T (PRC1) XP_011520494.1:n.1470+242C>T
XM_005254987.3:c.1672+687C>T (PRC1) XP_005255044.1:n.1672+687C>T
XM_006720759.2:c.*22+242C>T (PRC1) XP_006720822.1:n.*22+242C>T
XM_006720760.2:c.1672+687C>T (PRC1) XP_006720823.1:n.1672+687C>T
XM_011522187.2:c.1791+242C>T (PRC1) XP_011520489.1:n.1791+242C>T
XM_011522188.3:c.1749+610C>T (PRC1) XP_011520490.1:n.1749+610C>T
XM_011522189.2:c.1680+242C>T (PRC1) XP_011520491.1:n.1680+242C>T
XM_011522190.3:c.1620+242C>T (PRC1) XP_011520492.1:n.1620+242C>T
XM_011522191.3:c.*22+242C>T (PRC1) XP_011520493.1:n.*22+242C>T
XM_011522192.2:c.1470+242C>T (PRC1) XP_011520494.1:n.1470+242C>T
XM_017022712.2:c.1680+242C>T (PRC1) XP_016878201.1:n.1680+242C>T
XM_017022713.2:c.1638+610C>T (PRC1) XP_016878202.1:n.1638+610C>T
XM_017022714.2:c.1635+242C>T (PRC1) XP_016878203.1:n.1635+242C>T
XM_017022715.2:c.1635+242C>T (PRC1) XP_016878204.1:n.1635+242C>T
XM_017022716.2:c.1578+610C>T (PRC1) XP_016878205.1:n.1578+610C>T
XM_017022717.1:c.1516+687C>T (PRC1) XP_016878206.1:n.1516+687C>T
NM_003981.4:c.1791+242C>T (PRC1) MANE Select NP_003972.2:n.1791+242C>T
NM_001267580.2:c.1549+687C>T (PRC1) NP_001254509.2:n.1549+687C>T
NM_199413.3:c.1749+610C>T (PRC1) NP_955445.2:n.1749+610C>T