Canonical Allele Identifier: CA717053283

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs1410520417
• gnomAD v3: 15-90966782-A-G
• gnomAD v4: 15-90966782-A-G
• MyVariant Identifiers: chr15:g.91510012A>G (hg19) ; chr15:g.90966782A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966782A>G , CM000677.2:g.90966782A>G	GRCh38
NC_000015.9:g.91510012A>G , CM000677.1:g.91510012A>G	GRCh37
NC_000015.8:g.89311016A>G	NCBI36
NG_050647.1:g.32870T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*349T>C (PRC1) MANE Select	ENSP00000377793.3:n.*349T>C
ENST00000643536.1:c.*3974T>C	ENSP00000494429.1:n.*3974T>C
ENST00000361188.9:c.*349T>C (PRC1)	ENSP00000354679.5:n.*349T>C
ENST00000394249.7:c.*349T>C (PRC1)	ENSP00000377793.3:n.*349T>C
ENST00000555455.5:c.642-129T>C (PRC1)
ENST00000556972.6:c.125-129T>C (PRC1)	ENSP00000456737.1:n.125-129T>C
ENST00000560423.5:c.637T>C (PRC1)
NM_001267580.1:c.*392T>C (PRC1)	NP_001254509.1:n.*392T>C
NM_003981.3:c.*349T>C (PRC1)	NP_003972.1:n.*349T>C
NM_199413.2:c.*349T>C (PRC1)	NP_955445.1:n.*349T>C
NR_051984.1:n.310+104A>G (PRC1-AS1)
XM_005254987.1:c.*392T>C (PRC1)	XP_005255044.1:n.*392T>C
XM_006720759.1:c.*443T>C (PRC1)	XP_006720822.1:n.*443T>C
XM_006720760.1:c.1673-129T>C (PRC1)	XP_006720823.1:n.1673-129T>C
XM_011522187.1:c.1792-129T>C (PRC1)	XP_011520489.1:n.1792-129T>C
XM_011522188.1:c.1750-129T>C (PRC1)	XP_011520490.1:n.1750-129T>C
XM_011522189.1:c.1681-129T>C (PRC1)	XP_011520491.1:n.1681-129T>C
XM_011522190.1:c.1621-129T>C (PRC1)	XP_011520492.1:n.1621-129T>C
XM_011522191.1:c.*23-129T>C (PRC1)	XP_011520493.1:n.*23-129T>C
XM_011522192.1:c.1471-129T>C (PRC1)	XP_011520494.1:n.1471-129T>C
XM_005254987.3:c.*392T>C (PRC1)	XP_005255044.1:n.*392T>C
XM_006720759.2:c.*443T>C (PRC1)	XP_006720822.1:n.*443T>C
XM_006720760.2:c.1673-129T>C (PRC1)	XP_006720823.1:n.1673-129T>C
XM_011522187.2:c.1792-129T>C (PRC1)	XP_011520489.1:n.1792-129T>C
XM_011522188.3:c.1750-129T>C (PRC1)	XP_011520490.1:n.1750-129T>C
XM_011522189.2:c.1681-129T>C (PRC1)	XP_011520491.1:n.1681-129T>C
XM_011522190.3:c.1621-129T>C (PRC1)	XP_011520492.1:n.1621-129T>C
XM_011522191.3:c.*23-129T>C (PRC1)	XP_011520493.1:n.*23-129T>C
XM_011522192.2:c.1471-129T>C (PRC1)	XP_011520494.1:n.1471-129T>C
XM_017022712.2:c.*349T>C (PRC1)	XP_016878201.1:n.*349T>C
XM_017022713.2:c.*349T>C (PRC1)	XP_016878202.1:n.*349T>C
XM_017022714.2:c.1636-129T>C (PRC1)	XP_016878203.1:n.1636-129T>C
XM_017022715.2:c.*349T>C (PRC1)	XP_016878204.1:n.*349T>C
XM_017022716.2:c.*349T>C (PRC1)	XP_016878205.1:n.*349T>C
XM_017022717.1:c.*392T>C (PRC1)	XP_016878206.1:n.*392T>C
NM_003981.4:c.*349T>C (PRC1) MANE Select	NP_003972.2:n.*349T>C
NM_001267580.2:c.*392T>C (PRC1)	NP_001254509.2:n.*392T>C
NM_199413.3:c.*349T>C (PRC1)	NP_955445.2:n.*349T>C