Canonical Allele Identifier: CA972731149

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs2037521324
• gnomAD v3: 15-90966695-G-GAT
• gnomAD v4: 15-90966695-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966697_90966698dup , CM000677.2:g.90966697_90966698dup	GRCh38
NC_000015.9:g.91509927_91509928dup , CM000677.1:g.91509927_91509928dup	GRCh37
NC_000015.8:g.89310931_89310932dup	NCBI36
NG_050647.1:g.32955_32956dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*434_*435dup (PRC1) MANE Select	ENSP00000377793.3:n.*434_*435dup
ENST00000643536.1:c.*4059_*4060dup	ENSP00000494429.1:n.*4059_*4060dup
ENST00000361188.9:c.*434_*435dup (PRC1)	ENSP00000354679.5:n.*434_*435dup
ENST00000394249.7:c.*434_*435dup (PRC1)	ENSP00000377793.3:n.*434_*435dup
ENST00000555455.5:c.642-44_642-43dup (PRC1)
ENST00000556972.6:c.125-44_125-43dup (PRC1)	ENSP00000456737.1:n.125-44_125-43dup
ENST00000560423.5:c.722_723dup (PRC1)
NM_001267580.1:c.*477_*478dup (PRC1)	NP_001254509.1:n.*477_*478dup
NM_003981.3:c.*434_*435dup (PRC1)	NP_003972.1:n.*434_*435dup
NM_199413.2:c.*434_*435dup (PRC1)	NP_955445.1:n.*434_*435dup
NR_051984.1:n.310+19_310+20dup (PRC1-AS1)
XM_005254987.1:c.*477_*478dup (PRC1)	XP_005255044.1:n.*477_*478dup
XM_006720759.1:c.*528_*529dup (PRC1)	XP_006720822.1:n.*528_*529dup
XM_006720760.1:c.1673-44_1673-43dup (PRC1)	XP_006720823.1:n.1673-44_1673-43dup
XM_011522187.1:c.1792-44_1792-43dup (PRC1)	XP_011520489.1:n.1792-44_1792-43dup
XM_011522188.1:c.1750-44_1750-43dup (PRC1)	XP_011520490.1:n.1750-44_1750-43dup
XM_011522189.1:c.1681-44_1681-43dup (PRC1)	XP_011520491.1:n.1681-44_1681-43dup
XM_011522190.1:c.1621-44_1621-43dup (PRC1)	XP_011520492.1:n.1621-44_1621-43dup
XM_011522191.1:c.*23-44_*23-43dup (PRC1)	XP_011520493.1:n.*23-44_*23-43dup
XM_011522192.1:c.1471-44_1471-43dup (PRC1)	XP_011520494.1:n.1471-44_1471-43dup
XM_005254987.3:c.*477_*478dup (PRC1)	XP_005255044.1:n.*477_*478dup
XM_006720759.2:c.*528_*529dup (PRC1)	XP_006720822.1:n.*528_*529dup
XM_006720760.2:c.1673-44_1673-43dup (PRC1)	XP_006720823.1:n.1673-44_1673-43dup
XM_011522187.2:c.1792-44_1792-43dup (PRC1)	XP_011520489.1:n.1792-44_1792-43dup
XM_011522188.3:c.1750-44_1750-43dup (PRC1)	XP_011520490.1:n.1750-44_1750-43dup
XM_011522189.2:c.1681-44_1681-43dup (PRC1)	XP_011520491.1:n.1681-44_1681-43dup
XM_011522190.3:c.1621-44_1621-43dup (PRC1)	XP_011520492.1:n.1621-44_1621-43dup
XM_011522191.3:c.*23-44_*23-43dup (PRC1)	XP_011520493.1:n.*23-44_*23-43dup
XM_011522192.2:c.1471-44_1471-43dup (PRC1)	XP_011520494.1:n.1471-44_1471-43dup
XM_017022712.2:c.*434_*435dup (PRC1)	XP_016878201.1:n.*434_*435dup
XM_017022713.2:c.*434_*435dup (PRC1)	XP_016878202.1:n.*434_*435dup
XM_017022714.2:c.1636-44_1636-43dup (PRC1)	XP_016878203.1:n.1636-44_1636-43dup
XM_017022715.2:c.*434_*435dup (PRC1)	XP_016878204.1:n.*434_*435dup
XM_017022716.2:c.*434_*435dup (PRC1)	XP_016878205.1:n.*434_*435dup
XM_017022717.1:c.*477_*478dup (PRC1)	XP_016878206.1:n.*477_*478dup
NM_003981.4:c.*434_*435dup (PRC1) MANE Select	NP_003972.2:n.*434_*435dup
NM_001267580.2:c.*477_*478dup (PRC1)	NP_001254509.2:n.*477_*478dup
NM_199413.3:c.*434_*435dup (PRC1)	NP_955445.2:n.*434_*435dup