Canonical Allele Identifier: CA2195380787

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs2037518888

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966681_90966684dup , CM000677.2:g.90966681_90966684dup	GRCh38
NC_000015.9:g.91509911_91509914dup , CM000677.1:g.91509911_91509914dup	GRCh37
NC_000015.8:g.89310915_89310918dup	NCBI36
NG_050647.1:g.32968_32971dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*447_*450dup (PRC1) MANE Select	ENSP00000377793.3:n.*447_*450dup
ENST00000643536.1:c.*4072_*4075dup	ENSP00000494429.1:n.*4072_*4075dup
ENST00000361188.9:c.*447_*450dup (PRC1)	ENSP00000354679.5:n.*447_*450dup
ENST00000394249.7:c.*447_*450dup (PRC1)	ENSP00000377793.3:n.*447_*450dup
ENST00000555455.5:c.642-31_642-28dup (PRC1)
ENST00000556972.6:c.125-31_125-28dup (PRC1)	ENSP00000456737.1:n.125-31_125-28dup
ENST00000560423.5:c.735_738dup (PRC1)
NM_001267580.1:c.*490_*493dup (PRC1)	NP_001254509.1:n.*490_*493dup
NM_003981.3:c.*447_*450dup (PRC1)	NP_003972.1:n.*447_*450dup
NM_199413.2:c.*447_*450dup (PRC1)	NP_955445.1:n.*447_*450dup
NR_051984.1:n.310+3_310+6dup (PRC1-AS1)
XM_005254987.1:c.*490_*493dup (PRC1)	XP_005255044.1:n.*490_*493dup
XM_006720759.1:c.*541_*544dup (PRC1)	XP_006720822.1:n.*541_*544dup
XM_006720760.1:c.1673-31_1673-28dup (PRC1)	XP_006720823.1:n.1673-31_1673-28dup
XM_011522187.1:c.1792-31_1792-28dup (PRC1)	XP_011520489.1:n.1792-31_1792-28dup
XM_011522188.1:c.1750-31_1750-28dup (PRC1)	XP_011520490.1:n.1750-31_1750-28dup
XM_011522189.1:c.1681-31_1681-28dup (PRC1)	XP_011520491.1:n.1681-31_1681-28dup
XM_011522190.1:c.1621-31_1621-28dup (PRC1)	XP_011520492.1:n.1621-31_1621-28dup
XM_011522191.1:c.*23-31_*23-28dup (PRC1)	XP_011520493.1:n.*23-31_*23-28dup
XM_011522192.1:c.1471-31_1471-28dup (PRC1)	XP_011520494.1:n.1471-31_1471-28dup
XM_005254987.3:c.*490_*493dup (PRC1)	XP_005255044.1:n.*490_*493dup
XM_006720759.2:c.*541_*544dup (PRC1)	XP_006720822.1:n.*541_*544dup
XM_006720760.2:c.1673-31_1673-28dup (PRC1)	XP_006720823.1:n.1673-31_1673-28dup
XM_011522187.2:c.1792-31_1792-28dup (PRC1)	XP_011520489.1:n.1792-31_1792-28dup
XM_011522188.3:c.1750-31_1750-28dup (PRC1)	XP_011520490.1:n.1750-31_1750-28dup
XM_011522189.2:c.1681-31_1681-28dup (PRC1)	XP_011520491.1:n.1681-31_1681-28dup
XM_011522190.3:c.1621-31_1621-28dup (PRC1)	XP_011520492.1:n.1621-31_1621-28dup
XM_011522191.3:c.*23-31_*23-28dup (PRC1)	XP_011520493.1:n.*23-31_*23-28dup
XM_011522192.2:c.1471-31_1471-28dup (PRC1)	XP_011520494.1:n.1471-31_1471-28dup
XM_017022712.2:c.*447_*450dup (PRC1)	XP_016878201.1:n.*447_*450dup
XM_017022713.2:c.*447_*450dup (PRC1)	XP_016878202.1:n.*447_*450dup
XM_017022714.2:c.1636-31_1636-28dup (PRC1)	XP_016878203.1:n.1636-31_1636-28dup
XM_017022715.2:c.*447_*450dup (PRC1)	XP_016878204.1:n.*447_*450dup
XM_017022716.2:c.*447_*450dup (PRC1)	XP_016878205.1:n.*447_*450dup
XM_017022717.1:c.*490_*493dup (PRC1)	XP_016878206.1:n.*490_*493dup
NM_003981.4:c.*447_*450dup (PRC1) MANE Select	NP_003972.2:n.*447_*450dup
NM_001267580.2:c.*490_*493dup (PRC1)	NP_001254509.2:n.*490_*493dup
NM_199413.3:c.*447_*450dup (PRC1)	NP_955445.2:n.*447_*450dup