Canonical Allele Identifier: CA274771308

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs957739202
• gnomAD v2: 15-91509923-A-ATGAT
• gnomAD v3: 15-90966693-A-ATGAT
• gnomAD v4: 15-90966693-A-ATGAT
• MyVariant Identifiers: chr15:g.91509923_91509924insTGAT (hg19) ; chr15:g.90966693_90966694insTGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966694_90966697dup , CM000677.2:g.90966694_90966697dup	GRCh38
NC_000015.9:g.91509924_91509927dup , CM000677.1:g.91509924_91509927dup	GRCh37
NC_000015.8:g.89310928_89310931dup	NCBI36
NG_050647.1:g.32955_32958dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*434_*437dup (PRC1) MANE Select	ENSP00000377793.3:n.*434_*437dup
ENST00000643536.1:c.*4059_*4062dup	ENSP00000494429.1:n.*4059_*4062dup
ENST00000361188.9:c.*434_*437dup (PRC1)	ENSP00000354679.5:n.*434_*437dup
ENST00000394249.7:c.*434_*437dup (PRC1)	ENSP00000377793.3:n.*434_*437dup
ENST00000555455.5:c.642-44_642-41dup (PRC1)
ENST00000556972.6:c.125-44_125-41dup (PRC1)	ENSP00000456737.1:n.125-44_125-41dup
ENST00000560423.5:c.722_725dup (PRC1)
NM_001267580.1:c.*477_*480dup (PRC1)	NP_001254509.1:n.*477_*480dup
NM_003981.3:c.*434_*437dup (PRC1)	NP_003972.1:n.*434_*437dup
NM_199413.2:c.*434_*437dup (PRC1)	NP_955445.1:n.*434_*437dup
NR_051984.1:n.310+16_310+19dup (PRC1-AS1)
XM_005254987.1:c.*477_*480dup (PRC1)	XP_005255044.1:n.*477_*480dup
XM_006720759.1:c.*528_*531dup (PRC1)	XP_006720822.1:n.*528_*531dup
XM_006720760.1:c.1673-44_1673-41dup (PRC1)	XP_006720823.1:n.1673-44_1673-41dup
XM_011522187.1:c.1792-44_1792-41dup (PRC1)	XP_011520489.1:n.1792-44_1792-41dup
XM_011522188.1:c.1750-44_1750-41dup (PRC1)	XP_011520490.1:n.1750-44_1750-41dup
XM_011522189.1:c.1681-44_1681-41dup (PRC1)	XP_011520491.1:n.1681-44_1681-41dup
XM_011522190.1:c.1621-44_1621-41dup (PRC1)	XP_011520492.1:n.1621-44_1621-41dup
XM_011522191.1:c.*23-44_*23-41dup (PRC1)	XP_011520493.1:n.*23-44_*23-41dup
XM_011522192.1:c.1471-44_1471-41dup (PRC1)	XP_011520494.1:n.1471-44_1471-41dup
XM_005254987.3:c.*477_*480dup (PRC1)	XP_005255044.1:n.*477_*480dup
XM_006720759.2:c.*528_*531dup (PRC1)	XP_006720822.1:n.*528_*531dup
XM_006720760.2:c.1673-44_1673-41dup (PRC1)	XP_006720823.1:n.1673-44_1673-41dup
XM_011522187.2:c.1792-44_1792-41dup (PRC1)	XP_011520489.1:n.1792-44_1792-41dup
XM_011522188.3:c.1750-44_1750-41dup (PRC1)	XP_011520490.1:n.1750-44_1750-41dup
XM_011522189.2:c.1681-44_1681-41dup (PRC1)	XP_011520491.1:n.1681-44_1681-41dup
XM_011522190.3:c.1621-44_1621-41dup (PRC1)	XP_011520492.1:n.1621-44_1621-41dup
XM_011522191.3:c.*23-44_*23-41dup (PRC1)	XP_011520493.1:n.*23-44_*23-41dup
XM_011522192.2:c.1471-44_1471-41dup (PRC1)	XP_011520494.1:n.1471-44_1471-41dup
XM_017022712.2:c.*434_*437dup (PRC1)	XP_016878201.1:n.*434_*437dup
XM_017022713.2:c.*434_*437dup (PRC1)	XP_016878202.1:n.*434_*437dup
XM_017022714.2:c.1636-44_1636-41dup (PRC1)	XP_016878203.1:n.1636-44_1636-41dup
XM_017022715.2:c.*434_*437dup (PRC1)	XP_016878204.1:n.*434_*437dup
XM_017022716.2:c.*434_*437dup (PRC1)	XP_016878205.1:n.*434_*437dup
XM_017022717.1:c.*477_*480dup (PRC1)	XP_016878206.1:n.*477_*480dup
NM_003981.4:c.*434_*437dup (PRC1) MANE Select	NP_003972.2:n.*434_*437dup
NM_001267580.2:c.*477_*480dup (PRC1)	NP_001254509.2:n.*477_*480dup
NM_199413.3:c.*434_*437dup (PRC1)	NP_955445.2:n.*434_*437dup