Canonical Allele Identifier: CA2195380812

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs2037520904

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966694_90966695insTA , CM000677.2:g.90966694_90966695insTA	GRCh38
NC_000015.9:g.91509924_91509925insTA , CM000677.1:g.91509924_91509925insTA	GRCh37
NC_000015.8:g.89310928_89310929insTA	NCBI36
NG_050647.1:g.32957_32958insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*436_*437insTA (PRC1) MANE Select	ENSP00000377793.3:n.*436_*437insTA
ENST00000643536.1:c.*4061_*4062insTA	ENSP00000494429.1:n.*4061_*4062insTA
ENST00000361188.9:c.*436_*437insTA (PRC1)	ENSP00000354679.5:n.*436_*437insTA
ENST00000394249.7:c.*436_*437insTA (PRC1)	ENSP00000377793.3:n.*436_*437insTA
ENST00000555455.5:c.642-42_642-41insTA (PRC1)
ENST00000556972.6:c.125-42_125-41insTA (PRC1)	ENSP00000456737.1:n.125-42_125-41insTA
ENST00000560423.5:c.724_725insTA (PRC1)
NM_001267580.1:c.*479_*480insTA (PRC1)	NP_001254509.1:n.*479_*480insTA
NM_003981.3:c.*436_*437insTA (PRC1)	NP_003972.1:n.*436_*437insTA
NM_199413.2:c.*436_*437insTA (PRC1)	NP_955445.1:n.*436_*437insTA
NR_051984.1:n.310+16_310+17insTA (PRC1-AS1)
XM_005254987.1:c.*479_*480insTA (PRC1)	XP_005255044.1:n.*479_*480insTA
XM_006720759.1:c.*530_*531insTA (PRC1)	XP_006720822.1:n.*530_*531insTA
XM_006720760.1:c.1673-42_1673-41insTA (PRC1)	XP_006720823.1:n.1673-42_1673-41insTA
XM_011522187.1:c.1792-42_1792-41insTA (PRC1)	XP_011520489.1:n.1792-42_1792-41insTA
XM_011522188.1:c.1750-42_1750-41insTA (PRC1)	XP_011520490.1:n.1750-42_1750-41insTA
XM_011522189.1:c.1681-42_1681-41insTA (PRC1)	XP_011520491.1:n.1681-42_1681-41insTA
XM_011522190.1:c.1621-42_1621-41insTA (PRC1)	XP_011520492.1:n.1621-42_1621-41insTA
XM_011522191.1:c.*23-42_*23-41insTA (PRC1)	XP_011520493.1:n.*23-42_*23-41insTA
XM_011522192.1:c.1471-42_1471-41insTA (PRC1)	XP_011520494.1:n.1471-42_1471-41insTA
XM_005254987.3:c.*479_*480insTA (PRC1)	XP_005255044.1:n.*479_*480insTA
XM_006720759.2:c.*530_*531insTA (PRC1)	XP_006720822.1:n.*530_*531insTA
XM_006720760.2:c.1673-42_1673-41insTA (PRC1)	XP_006720823.1:n.1673-42_1673-41insTA
XM_011522187.2:c.1792-42_1792-41insTA (PRC1)	XP_011520489.1:n.1792-42_1792-41insTA
XM_011522188.3:c.1750-42_1750-41insTA (PRC1)	XP_011520490.1:n.1750-42_1750-41insTA
XM_011522189.2:c.1681-42_1681-41insTA (PRC1)	XP_011520491.1:n.1681-42_1681-41insTA
XM_011522190.3:c.1621-42_1621-41insTA (PRC1)	XP_011520492.1:n.1621-42_1621-41insTA
XM_011522191.3:c.*23-42_*23-41insTA (PRC1)	XP_011520493.1:n.*23-42_*23-41insTA
XM_011522192.2:c.1471-42_1471-41insTA (PRC1)	XP_011520494.1:n.1471-42_1471-41insTA
XM_017022712.2:c.*436_*437insTA (PRC1)	XP_016878201.1:n.*436_*437insTA
XM_017022713.2:c.*436_*437insTA (PRC1)	XP_016878202.1:n.*436_*437insTA
XM_017022714.2:c.1636-42_1636-41insTA (PRC1)	XP_016878203.1:n.1636-42_1636-41insTA
XM_017022715.2:c.*436_*437insTA (PRC1)	XP_016878204.1:n.*436_*437insTA
XM_017022716.2:c.*436_*437insTA (PRC1)	XP_016878205.1:n.*436_*437insTA
XM_017022717.1:c.*479_*480insTA (PRC1)	XP_016878206.1:n.*479_*480insTA
NM_003981.4:c.*436_*437insTA (PRC1) MANE Select	NP_003972.2:n.*436_*437insTA
NM_001267580.2:c.*479_*480insTA (PRC1)	NP_001254509.2:n.*479_*480insTA
NM_199413.3:c.*436_*437insTA (PRC1)	NP_955445.2:n.*436_*437insTA