Canonical Allele Identifier: CA492187509
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.91509731T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966501T>C , CM000677.2:g.90966501T>C GRCh38
NC_000015.9:g.91509731T>C , CM000677.1:g.91509731T>C GRCh37
NC_000015.8:g.89310735T>C NCBI36
NG_050647.1:g.33151A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*630A>G (PRC1) MANE Select ENSP00000377793.3:n.*630A>G
ENST00000643536.1:c.*4255A>G ENSP00000494429.1:n.*4255A>G
ENST00000361188.9:c.*630A>G (PRC1) ENSP00000354679.5:n.*630A>G
ENST00000394249.7:c.*630A>G (PRC1) ENSP00000377793.3:n.*630A>G
ENST00000555455.5:c.794A>G (PRC1)
ENST00000556972.6:c.277A>G (PRC1) ENSP00000456737.1:n.277A>G
NM_001267580.1:c.*673A>G (PRC1) NP_001254509.1:n.*673A>G
NM_003981.3:c.*630A>G (PRC1) NP_003972.1:n.*630A>G
NM_199413.2:c.*630A>G (PRC1) NP_955445.1:n.*630A>G
NR_051984.1:n.133T>C (PRC1-AS1)
XM_005254987.1:c.*673A>G (PRC1) XP_005255044.1:n.*673A>G
XM_006720759.1:c.*724A>G (PRC1) XP_006720822.1:n.*724A>G
XM_006720760.1:c.*136A>G (PRC1) XP_006720823.1:n.*136A>G
XM_011522187.1:c.*78A>G (PRC1) XP_011520489.1:n.*78A>G
XM_011522188.1:c.*78A>G (PRC1) XP_011520490.1:n.*78A>G
XM_011522189.1:c.*78A>G (PRC1) XP_011520491.1:n.*78A>G
XM_011522190.1:c.*78A>G (PRC1) XP_011520492.1:n.*78A>G
XM_011522192.1:c.*78A>G (PRC1) XP_011520494.1:n.*78A>G
XM_005254987.3:c.*673A>G (PRC1) XP_005255044.1:n.*673A>G
XM_006720759.2:c.*724A>G (PRC1) XP_006720822.1:n.*724A>G
XM_006720760.2:c.*136A>G (PRC1) XP_006720823.1:n.*136A>G
XM_011522187.2:c.*78A>G (PRC1) XP_011520489.1:n.*78A>G
XM_011522188.3:c.*78A>G (PRC1) XP_011520490.1:n.*78A>G
XM_011522189.2:c.*78A>G (PRC1) XP_011520491.1:n.*78A>G
XM_011522191.3:c.*175A>G (PRC1) XP_011520493.1:n.*175A>G
XM_011522192.2:c.*78A>G (PRC1) XP_011520494.1:n.*78A>G
XM_017022712.2:c.*630A>G (PRC1) XP_016878201.1:n.*630A>G
XM_017022713.2:c.*630A>G (PRC1) XP_016878202.1:n.*630A>G
XM_017022715.2:c.*630A>G (PRC1) XP_016878204.1:n.*630A>G
XM_017022716.2:c.*630A>G (PRC1) XP_016878205.1:n.*630A>G
XM_017022717.1:c.*673A>G (PRC1) XP_016878206.1:n.*673A>G
NM_003981.4:c.*630A>G (PRC1) MANE Select NP_003972.2:n.*630A>G
NM_001267580.2:c.*673A>G (PRC1) NP_001254509.2:n.*673A>G
NM_199413.3:c.*630A>G (PRC1) NP_955445.2:n.*630A>G