Canonical Allele Identifier: CA972731173

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs2037524877
• gnomAD v3: 15-90966731-AAAG-A
• gnomAD v4: 15-90966731-AAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966733_90966735del , CM000677.2:g.90966733_90966735del	GRCh38
NC_000015.9:g.91509963_91509965del , CM000677.1:g.91509963_91509965del	GRCh37
NC_000015.8:g.89310967_89310969del	NCBI36
NG_050647.1:g.32918_32920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*397_*399del (PRC1) MANE Select	ENSP00000377793.3:n.*397_*399del
ENST00000643536.1:c.*4022_*4024del	ENSP00000494429.1:n.*4022_*4024del
ENST00000361188.9:c.*397_*399del (PRC1)	ENSP00000354679.5:n.*397_*399del
ENST00000394249.7:c.*397_*399del (PRC1)	ENSP00000377793.3:n.*397_*399del
ENST00000555455.5:c.642-81_642-79del (PRC1)
ENST00000556972.6:c.125-81_125-79del (PRC1)	ENSP00000456737.1:n.125-81_125-79del
ENST00000560423.5:c.685_687del (PRC1)
NM_001267580.1:c.*440_*442del (PRC1)	NP_001254509.1:n.*440_*442del
NM_003981.3:c.*397_*399del (PRC1)	NP_003972.1:n.*397_*399del
NM_199413.2:c.*397_*399del (PRC1)	NP_955445.1:n.*397_*399del
NR_051984.1:n.310+55_310+57del (PRC1-AS1)
XM_005254987.1:c.*440_*442del (PRC1)	XP_005255044.1:n.*440_*442del
XM_006720759.1:c.*491_*493del (PRC1)	XP_006720822.1:n.*491_*493del
XM_006720760.1:c.1673-81_1673-79del (PRC1)	XP_006720823.1:n.1673-81_1673-79del
XM_011522187.1:c.1792-81_1792-79del (PRC1)	XP_011520489.1:n.1792-81_1792-79del
XM_011522188.1:c.1750-81_1750-79del (PRC1)	XP_011520490.1:n.1750-81_1750-79del
XM_011522189.1:c.1681-81_1681-79del (PRC1)	XP_011520491.1:n.1681-81_1681-79del
XM_011522190.1:c.1621-81_1621-79del (PRC1)	XP_011520492.1:n.1621-81_1621-79del
XM_011522191.1:c.*23-81_*23-79del (PRC1)	XP_011520493.1:n.*23-81_*23-79del
XM_011522192.1:c.1471-81_1471-79del (PRC1)	XP_011520494.1:n.1471-81_1471-79del
XM_005254987.3:c.*440_*442del (PRC1)	XP_005255044.1:n.*440_*442del
XM_006720759.2:c.*491_*493del (PRC1)	XP_006720822.1:n.*491_*493del
XM_006720760.2:c.1673-81_1673-79del (PRC1)	XP_006720823.1:n.1673-81_1673-79del
XM_011522187.2:c.1792-81_1792-79del (PRC1)	XP_011520489.1:n.1792-81_1792-79del
XM_011522188.3:c.1750-81_1750-79del (PRC1)	XP_011520490.1:n.1750-81_1750-79del
XM_011522189.2:c.1681-81_1681-79del (PRC1)	XP_011520491.1:n.1681-81_1681-79del
XM_011522190.3:c.1621-81_1621-79del (PRC1)	XP_011520492.1:n.1621-81_1621-79del
XM_011522191.3:c.*23-81_*23-79del (PRC1)	XP_011520493.1:n.*23-81_*23-79del
XM_011522192.2:c.1471-81_1471-79del (PRC1)	XP_011520494.1:n.1471-81_1471-79del
XM_017022712.2:c.*397_*399del (PRC1)	XP_016878201.1:n.*397_*399del
XM_017022713.2:c.*397_*399del (PRC1)	XP_016878202.1:n.*397_*399del
XM_017022714.2:c.1636-81_1636-79del (PRC1)	XP_016878203.1:n.1636-81_1636-79del
XM_017022715.2:c.*397_*399del (PRC1)	XP_016878204.1:n.*397_*399del
XM_017022716.2:c.*397_*399del (PRC1)	XP_016878205.1:n.*397_*399del
XM_017022717.1:c.*440_*442del (PRC1)	XP_016878206.1:n.*440_*442del
NM_003981.4:c.*397_*399del (PRC1) MANE Select	NP_003972.2:n.*397_*399del
NM_001267580.2:c.*440_*442del (PRC1)	NP_001254509.2:n.*440_*442del
NM_199413.3:c.*397_*399del (PRC1)	NP_955445.2:n.*397_*399del