Canonical Allele Identifier: CA2195380986
Gene: PRC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966205C= , CM000677.2:g.90966205C= GRCh38
NC_000015.9:g.91509435C= , CM000677.1:g.91509435C= GRCh37
NC_000015.8:g.89310439C= NCBI36
NG_050647.1:g.33447G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*926G= MANE Select ENSP00000377793.3:n.*926G=
ENST00000643536.1:c.*4551G= ENSP00000494429.1:n.*4551G=
ENST00000361188.9:c.*926G= ENSP00000354679.5:n.*926G=
ENST00000394249.7:c.*926G= ENSP00000377793.3:n.*926G=
ENST00000556972.6:c.573G= ENSP00000456737.1:n.573G=
NM_001267580.1:c.*969G= NP_001254509.1:n.*969G=
NM_003981.3:c.*926G= NP_003972.1:n.*926G=
NM_199413.2:c.*926G= NP_955445.1:n.*926G=
XM_005254987.1:c.*969G= XP_005255044.1:n.*969G=
XM_006720759.1:c.*1020G= XP_006720822.1:n.*1020G=
XM_006720760.1:c.*432G= XP_006720823.1:n.*432G=
XM_011522187.1:c.*374G= XP_011520489.1:n.*374G=
XM_011522188.1:c.*374G= XP_011520490.1:n.*374G=
XM_011522189.1:c.*374G= XP_011520491.1:n.*374G=
XM_011522190.1:c.*374G= XP_011520492.1:n.*374G=
XM_011522192.1:c.*374G= XP_011520494.1:n.*374G=
XM_005254987.3:c.*969G= XP_005255044.1:n.*969G=
XM_006720759.2:c.*1020G= XP_006720822.1:n.*1020G=
XM_006720760.2:c.*432G= XP_006720823.1:n.*432G=
XM_011522187.2:c.*374G= XP_011520489.1:n.*374G=
XM_011522188.3:c.*374G= XP_011520490.1:n.*374G=
XM_011522189.2:c.*374G= XP_011520491.1:n.*374G=
XM_011522191.3:c.*471G= XP_011520493.1:n.*471G=
XM_011522192.2:c.*374G= XP_011520494.1:n.*374G=
XM_017022712.2:c.*926G= XP_016878201.1:n.*926G=
XM_017022713.2:c.*926G= XP_016878202.1:n.*926G=
XM_017022715.2:c.*926G= XP_016878204.1:n.*926G=
XM_017022716.2:c.*926G= XP_016878205.1:n.*926G=
XM_017022717.1:c.*969G= XP_016878206.1:n.*969G=
NM_003981.4:c.*926G= MANE Select NP_003972.2:n.*926G=
NM_001267580.2:c.*969G= NP_001254509.2:n.*969G=
NM_199413.3:c.*926G= NP_955445.2:n.*926G=