Canonical Allele Identifier: CA273812
Gene: PRC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 157646
ClinVar RCV Id: RCV000162271
dbSNP Id: rs7601

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966362T>C , CM000677.2:g.90966362T>C GRCh38
NC_000015.9:g.91509592T>C , CM000677.1:g.91509592T>C GRCh37
NC_000015.8:g.89310596T>C NCBI36
NG_050647.1:g.33290A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000394249.8:c.*769A>G MANE Select ENSP00000377793.3:n.*769A>G
ENST00000643536.1:c.*4394A>G ENSP00000494429.1:n.*4394A>G
ENST00000361188.9:c.*769A>G ENSP00000354679.5:n.*769A>G
ENST00000394249.7:c.*769A>G ENSP00000377793.3:n.*769A>G
ENST00000556972.6:c.416A>G ENSP00000456737.1:n.416A>G
NM_001267580.1:c.*812A>G NP_001254509.1:n.*812A>G
NM_003981.3:c.*769A>G NP_003972.1:n.*769A>G
NM_199413.2:c.*769A>G NP_955445.1:n.*769A>G
XM_005254987.1:c.*812A>G XP_005255044.1:n.*812A>G
XM_006720759.1:c.*863A>G XP_006720822.1:n.*863A>G
XM_006720760.1:c.*275A>G XP_006720823.1:n.*275A>G
XM_011522187.1:c.*217A>G XP_011520489.1:n.*217A>G
XM_011522188.1:c.*217A>G XP_011520490.1:n.*217A>G
XM_011522189.1:c.*217A>G XP_011520491.1:n.*217A>G
XM_011522190.1:c.*217A>G XP_011520492.1:n.*217A>G
XM_011522192.1:c.*217A>G XP_011520494.1:n.*217A>G
XM_005254987.3:c.*812A>G XP_005255044.1:n.*812A>G
XM_006720759.2:c.*863A>G XP_006720822.1:n.*863A>G
XM_006720760.2:c.*275A>G XP_006720823.1:n.*275A>G
XM_011522187.2:c.*217A>G XP_011520489.1:n.*217A>G
XM_011522188.3:c.*217A>G XP_011520490.1:n.*217A>G
XM_011522189.2:c.*217A>G XP_011520491.1:n.*217A>G
XM_011522191.3:c.*314A>G XP_011520493.1:n.*314A>G
XM_011522192.2:c.*217A>G XP_011520494.1:n.*217A>G
XM_017022712.2:c.*769A>G XP_016878201.1:n.*769A>G
XM_017022713.2:c.*769A>G XP_016878202.1:n.*769A>G
XM_017022715.2:c.*769A>G XP_016878204.1:n.*769A>G
XM_017022716.2:c.*769A>G XP_016878205.1:n.*769A>G
XM_017022717.1:c.*812A>G XP_016878206.1:n.*812A>G
NM_003981.4:c.*769A>G MANE Select NP_003972.2:n.*769A>G
NM_001267580.2:c.*812A>G NP_001254509.2:n.*812A>G
NM_199413.3:c.*769A>G NP_955445.2:n.*769A>G