Canonical Allele Identifier: CA492187877

Gene: PRC1 PRC1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.91509850A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966620A>C , CM000677.2:g.90966620A>C	GRCh38
NC_000015.9:g.91509850A>C , CM000677.1:g.91509850A>C	GRCh37
NC_000015.8:g.89310854A>C	NCBI36
NG_050647.1:g.33032T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*511T>G (PRC1) MANE Select	ENSP00000377793.3:n.*511T>G
ENST00000643536.1:c.*4136T>G	ENSP00000494429.1:n.*4136T>G
ENST00000361188.9:c.*511T>G (PRC1)	ENSP00000354679.5:n.*511T>G
ENST00000394249.7:c.*511T>G (PRC1)	ENSP00000377793.3:n.*511T>G
ENST00000555455.5:c.675T>G (PRC1)
ENST00000556972.6:c.158T>G (PRC1)	ENSP00000456737.1:n.158T>G
NM_001267580.1:c.*554T>G (PRC1)	NP_001254509.1:n.*554T>G
NM_003981.3:c.*511T>G (PRC1)	NP_003972.1:n.*511T>G
NM_199413.2:c.*511T>G (PRC1)	NP_955445.1:n.*511T>G
NR_051984.1:n.252A>C (PRC1-AS1)
XM_005254987.1:c.*554T>G (PRC1)	XP_005255044.1:n.*554T>G
XM_006720759.1:c.*605T>G (PRC1)	XP_006720822.1:n.*605T>G
XM_006720760.1:c.*17T>G (PRC1)	XP_006720823.1:n.*17T>G
XM_011522187.1:c.1825T>G (PRC1)	XP_011520489.1:p.Cys609Gly
XM_011522188.1:c.1783T>G (PRC1)	XP_011520490.1:p.Cys595Gly
XM_011522189.1:c.1714T>G (PRC1)	XP_011520491.1:p.Cys572Gly
XM_011522190.1:c.1654T>G (PRC1)	XP_011520492.1:p.Cys552Gly
XM_011522191.1:c.*56T>G (PRC1)	XP_011520493.1:n.*56T>G
XM_011522192.1:c.1504T>G (PRC1)	XP_011520494.1:p.Cys502Gly
XM_005254987.3:c.*554T>G (PRC1)	XP_005255044.1:n.*554T>G
XM_006720759.2:c.*605T>G (PRC1)	XP_006720822.1:n.*605T>G
XM_006720760.2:c.*17T>G (PRC1)	XP_006720823.1:n.*17T>G
XM_011522187.2:c.1825T>G (PRC1)	XP_011520489.1:p.Cys609Gly
XM_011522188.3:c.1783T>G (PRC1)	XP_011520490.1:p.Cys595Gly
XM_011522189.2:c.1714T>G (PRC1)	XP_011520491.1:p.Cys572Gly
XM_011522190.3:c.1654T>G (PRC1)	XP_011520492.1:p.Cys552Gly
XM_011522191.3:c.*56T>G (PRC1)	XP_011520493.1:n.*56T>G
XM_011522192.2:c.1504T>G (PRC1)	XP_011520494.1:p.Cys502Gly
XM_017022712.2:c.*511T>G (PRC1)	XP_016878201.1:n.*511T>G
XM_017022713.2:c.*511T>G (PRC1)	XP_016878202.1:n.*511T>G
XM_017022714.2:c.1669T>G (PRC1)	XP_016878203.1:p.Cys557Gly
XM_017022715.2:c.*511T>G (PRC1)	XP_016878204.1:n.*511T>G
XM_017022716.2:c.*511T>G (PRC1)	XP_016878205.1:n.*511T>G
XM_017022717.1:c.*554T>G (PRC1)	XP_016878206.1:n.*554T>G
NM_003981.4:c.*511T>G (PRC1) MANE Select	NP_003972.2:n.*511T>G
NM_001267580.2:c.*554T>G (PRC1)	NP_001254509.2:n.*554T>G
NM_199413.3:c.*511T>G (PRC1)	NP_955445.2:n.*511T>G