Canonical Allele Identifier: CA2630414321

Gene: PRC1 PRC1-AS1

Linked Data

• gnomAD v4: 15-90966371-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966371A>G , CM000677.2:g.90966371A>G	GRCh38
NC_000015.9:g.91509601A>G , CM000677.1:g.91509601A>G	GRCh37
NC_000015.8:g.89310605A>G	NCBI36
NG_050647.1:g.33281T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394249.8:c.*760T>C (PRC1) MANE Select	ENSP00000377793.3:n.*760T>C
ENST00000643536.1:c.*4385T>C	ENSP00000494429.1:n.*4385T>C
ENST00000361188.9:c.*760T>C (PRC1)	ENSP00000354679.5:n.*760T>C
ENST00000394249.7:c.*760T>C (PRC1)	ENSP00000377793.3:n.*760T>C
ENST00000556972.6:c.407T>C (PRC1)	ENSP00000456737.1:n.407T>C
NM_001267580.1:c.*803T>C (PRC1)	NP_001254509.1:n.*803T>C
NM_003981.3:c.*760T>C (PRC1)	NP_003972.1:n.*760T>C
NM_199413.2:c.*760T>C (PRC1)	NP_955445.1:n.*760T>C
NR_051984.1:n.3A>G (PRC1-AS1)
XM_005254987.1:c.*803T>C (PRC1)	XP_005255044.1:n.*803T>C
XM_006720759.1:c.*854T>C (PRC1)	XP_006720822.1:n.*854T>C
XM_006720760.1:c.*266T>C (PRC1)	XP_006720823.1:n.*266T>C
XM_011522187.1:c.*208T>C (PRC1)	XP_011520489.1:n.*208T>C
XM_011522188.1:c.*208T>C (PRC1)	XP_011520490.1:n.*208T>C
XM_011522189.1:c.*208T>C (PRC1)	XP_011520491.1:n.*208T>C
XM_011522190.1:c.*208T>C (PRC1)	XP_011520492.1:n.*208T>C
XM_011522192.1:c.*208T>C (PRC1)	XP_011520494.1:n.*208T>C
XM_005254987.3:c.*803T>C (PRC1)	XP_005255044.1:n.*803T>C
XM_006720759.2:c.*854T>C (PRC1)	XP_006720822.1:n.*854T>C
XM_006720760.2:c.*266T>C (PRC1)	XP_006720823.1:n.*266T>C
XM_011522187.2:c.*208T>C (PRC1)	XP_011520489.1:n.*208T>C
XM_011522188.3:c.*208T>C (PRC1)	XP_011520490.1:n.*208T>C
XM_011522189.2:c.*208T>C (PRC1)	XP_011520491.1:n.*208T>C
XM_011522191.3:c.*305T>C (PRC1)	XP_011520493.1:n.*305T>C
XM_011522192.2:c.*208T>C (PRC1)	XP_011520494.1:n.*208T>C
XM_017022712.2:c.*760T>C (PRC1)	XP_016878201.1:n.*760T>C
XM_017022713.2:c.*760T>C (PRC1)	XP_016878202.1:n.*760T>C
XM_017022715.2:c.*760T>C (PRC1)	XP_016878204.1:n.*760T>C
XM_017022716.2:c.*760T>C (PRC1)	XP_016878205.1:n.*760T>C
XM_017022717.1:c.*803T>C (PRC1)	XP_016878206.1:n.*803T>C
NM_003981.4:c.*760T>C (PRC1) MANE Select	NP_003972.2:n.*760T>C
NM_001267580.2:c.*803T>C (PRC1)	NP_001254509.2:n.*803T>C
NM_199413.3:c.*760T>C (PRC1)	NP_955445.2:n.*760T>C