Canonical Allele Identifier: CA273810

Gene: PRC1 PRC1-AS1

Linked Data

• ClinVar Variation Id: 157644
• ClinVar RCV Id: RCV000162269
• dbSNP Id: rs12910825
• gnomAD v2: 15-91511260-A-G
• gnomAD v3: 15-90968030-A-G
• gnomAD v4: 15-90968030-A-G
• MyVariant Identifiers: chr15:g.91511260A>G (hg19) ; chr15:g.90968030A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90968030A>G , CM000677.2:g.90968030A>G	GRCh38
NC_000015.9:g.91511260A>G , CM000677.1:g.91511260A>G	GRCh37
NC_000015.8:g.89312264A>G	NCBI36
NG_050647.1:g.31622T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.1792-828T>C (PRC1) MANE Select	ENSP00000377793.3:n.1792-828T>C
ENST00000643536.1:c.*2726T>C	ENSP00000494429.1:n.*2726T>C
ENST00000361188.9:c.1750-828T>C (PRC1)	ENSP00000354679.5:n.1750-828T>C
ENST00000394249.7:c.1792-828T>C (PRC1)	ENSP00000377793.3:n.1792-828T>C
ENST00000442656.6:c.1550-828T>C (PRC1)	ENSP00000409549.2:n.1550-828T>C
ENST00000555455.5:c.641+1049T>C (PRC1)
ENST00000556972.6:c.125-1377T>C (PRC1)	ENSP00000456737.1:n.125-1377T>C
ENST00000560423.5:c.217-828T>C (PRC1)
NM_001267580.1:c.1550-828T>C (PRC1)	NP_001254509.1:n.1550-828T>C
NM_003981.3:c.1792-828T>C (PRC1)	NP_003972.1:n.1792-828T>C
NM_199413.2:c.1750-828T>C (PRC1)	NP_955445.1:n.1750-828T>C
NR_051984.1:n.310+1352A>G (PRC1-AS1)
XM_005254987.1:c.1673-828T>C (PRC1)	XP_005255044.1:n.1673-828T>C
XM_006720759.1:c.*23-828T>C (PRC1)	XP_006720822.1:n.*23-828T>C
XM_006720760.1:c.1673-1377T>C (PRC1)	XP_006720823.1:n.1673-1377T>C
XM_011522187.1:c.1791+1049T>C (PRC1)	XP_011520489.1:n.1791+1049T>C
XM_011522188.1:c.1750-1377T>C (PRC1)	XP_011520490.1:n.1750-1377T>C
XM_011522189.1:c.1680+1049T>C (PRC1)	XP_011520491.1:n.1680+1049T>C
XM_011522190.1:c.1620+1049T>C (PRC1)	XP_011520492.1:n.1620+1049T>C
XM_011522191.1:c.*22+1049T>C (PRC1)	XP_011520493.1:n.*22+1049T>C
XM_011522192.1:c.1470+1049T>C (PRC1)	XP_011520494.1:n.1470+1049T>C
XM_005254987.3:c.1673-828T>C (PRC1)	XP_005255044.1:n.1673-828T>C
XM_006720759.2:c.*23-828T>C (PRC1)	XP_006720822.1:n.*23-828T>C
XM_006720760.2:c.1673-1377T>C (PRC1)	XP_006720823.1:n.1673-1377T>C
XM_011522187.2:c.1791+1049T>C (PRC1)	XP_011520489.1:n.1791+1049T>C
XM_011522188.3:c.1750-1377T>C (PRC1)	XP_011520490.1:n.1750-1377T>C
XM_011522189.2:c.1680+1049T>C (PRC1)	XP_011520491.1:n.1680+1049T>C
XM_011522190.3:c.1620+1049T>C (PRC1)	XP_011520492.1:n.1620+1049T>C
XM_011522191.3:c.*22+1049T>C (PRC1)	XP_011520493.1:n.*22+1049T>C
XM_011522192.2:c.1470+1049T>C (PRC1)	XP_011520494.1:n.1470+1049T>C
XM_017022712.2:c.1681-828T>C (PRC1)	XP_016878201.1:n.1681-828T>C
XM_017022713.2:c.1639-828T>C (PRC1)	XP_016878202.1:n.1639-828T>C
XM_017022714.2:c.1635+1049T>C (PRC1)	XP_016878203.1:n.1635+1049T>C
XM_017022715.2:c.1636-828T>C (PRC1)	XP_016878204.1:n.1636-828T>C
XM_017022716.2:c.1579-828T>C (PRC1)	XP_016878205.1:n.1579-828T>C
XM_017022717.1:c.1517-828T>C (PRC1)	XP_016878206.1:n.1517-828T>C
NM_003981.4:c.1792-828T>C (PRC1) MANE Select	NP_003972.2:n.1792-828T>C
NM_001267580.2:c.1550-828T>C (PRC1)	NP_001254509.2:n.1550-828T>C
NM_199413.3:c.1750-828T>C (PRC1)	NP_955445.2:n.1750-828T>C