Canonical Allele Identifier: CA492187496
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.91509727T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966497T>G , CM000677.2:g.90966497T>G GRCh38
NC_000015.9:g.91509727T>G , CM000677.1:g.91509727T>G GRCh37
NC_000015.8:g.89310731T>G NCBI36
NG_050647.1:g.33155A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*634A>C (PRC1) MANE Select ENSP00000377793.3:n.*634A>C
ENST00000643536.1:c.*4259A>C ENSP00000494429.1:n.*4259A>C
ENST00000361188.9:c.*634A>C (PRC1) ENSP00000354679.5:n.*634A>C
ENST00000394249.7:c.*634A>C (PRC1) ENSP00000377793.3:n.*634A>C
ENST00000555455.5:c.798A>C (PRC1)
ENST00000556972.6:c.281A>C (PRC1) ENSP00000456737.1:n.281A>C
NM_001267580.1:c.*677A>C (PRC1) NP_001254509.1:n.*677A>C
NM_003981.3:c.*634A>C (PRC1) NP_003972.1:n.*634A>C
NM_199413.2:c.*634A>C (PRC1) NP_955445.1:n.*634A>C
NR_051984.1:n.129T>G (PRC1-AS1)
XM_005254987.1:c.*677A>C (PRC1) XP_005255044.1:n.*677A>C
XM_006720759.1:c.*728A>C (PRC1) XP_006720822.1:n.*728A>C
XM_006720760.1:c.*140A>C (PRC1) XP_006720823.1:n.*140A>C
XM_011522187.1:c.*82A>C (PRC1) XP_011520489.1:n.*82A>C
XM_011522188.1:c.*82A>C (PRC1) XP_011520490.1:n.*82A>C
XM_011522189.1:c.*82A>C (PRC1) XP_011520491.1:n.*82A>C
XM_011522190.1:c.*82A>C (PRC1) XP_011520492.1:n.*82A>C
XM_011522192.1:c.*82A>C (PRC1) XP_011520494.1:n.*82A>C
XM_005254987.3:c.*677A>C (PRC1) XP_005255044.1:n.*677A>C
XM_006720759.2:c.*728A>C (PRC1) XP_006720822.1:n.*728A>C
XM_006720760.2:c.*140A>C (PRC1) XP_006720823.1:n.*140A>C
XM_011522187.2:c.*82A>C (PRC1) XP_011520489.1:n.*82A>C
XM_011522188.3:c.*82A>C (PRC1) XP_011520490.1:n.*82A>C
XM_011522189.2:c.*82A>C (PRC1) XP_011520491.1:n.*82A>C
XM_011522191.3:c.*179A>C (PRC1) XP_011520493.1:n.*179A>C
XM_011522192.2:c.*82A>C (PRC1) XP_011520494.1:n.*82A>C
XM_017022712.2:c.*634A>C (PRC1) XP_016878201.1:n.*634A>C
XM_017022713.2:c.*634A>C (PRC1) XP_016878202.1:n.*634A>C
XM_017022715.2:c.*634A>C (PRC1) XP_016878204.1:n.*634A>C
XM_017022716.2:c.*634A>C (PRC1) XP_016878205.1:n.*634A>C
XM_017022717.1:c.*677A>C (PRC1) XP_016878206.1:n.*677A>C
NM_003981.4:c.*634A>C (PRC1) MANE Select NP_003972.2:n.*634A>C
NM_001267580.2:c.*677A>C (PRC1) NP_001254509.2:n.*677A>C
NM_199413.3:c.*634A>C (PRC1) NP_955445.2:n.*634A>C