Canonical Allele Identifier: CA492187822

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs2037509179
• gnomAD v4: 15-90966602-G-A
• MyVariant Identifiers: chr15:g.91509832G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966602G>A , CM000677.2:g.90966602G>A	GRCh38
NC_000015.9:g.91509832G>A , CM000677.1:g.91509832G>A	GRCh37
NC_000015.8:g.89310836G>A	NCBI36
NG_050647.1:g.33050C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*529C>T (PRC1) MANE Select	ENSP00000377793.3:n.*529C>T
ENST00000643536.1:c.*4154C>T	ENSP00000494429.1:n.*4154C>T
ENST00000361188.9:c.*529C>T (PRC1)	ENSP00000354679.5:n.*529C>T
ENST00000394249.7:c.*529C>T (PRC1)	ENSP00000377793.3:n.*529C>T
ENST00000555455.5:c.693C>T (PRC1)
ENST00000556972.6:c.176C>T (PRC1)	ENSP00000456737.1:n.176C>T
NM_001267580.1:c.*572C>T (PRC1)	NP_001254509.1:n.*572C>T
NM_003981.3:c.*529C>T (PRC1)	NP_003972.1:n.*529C>T
NM_199413.2:c.*529C>T (PRC1)	NP_955445.1:n.*529C>T
NR_051984.1:n.234G>A (PRC1-AS1)
XM_005254987.1:c.*572C>T (PRC1)	XP_005255044.1:n.*572C>T
XM_006720759.1:c.*623C>T (PRC1)	XP_006720822.1:n.*623C>T
XM_006720760.1:c.*35C>T (PRC1)	XP_006720823.1:n.*35C>T
XM_011522187.1:c.1843C>T (PRC1)	XP_011520489.1:p.Pro615Ser
XM_011522188.1:c.1801C>T (PRC1)	XP_011520490.1:p.Pro601Ser
XM_011522189.1:c.1732C>T (PRC1)	XP_011520491.1:p.Pro578Ser
XM_011522190.1:c.1672C>T (PRC1)	XP_011520492.1:p.Pro558Ser
XM_011522191.1:c.*74C>T (PRC1)	XP_011520493.1:n.*74C>T
XM_011522192.1:c.1522C>T (PRC1)	XP_011520494.1:p.Pro508Ser
XM_005254987.3:c.*572C>T (PRC1)	XP_005255044.1:n.*572C>T
XM_006720759.2:c.*623C>T (PRC1)	XP_006720822.1:n.*623C>T
XM_006720760.2:c.*35C>T (PRC1)	XP_006720823.1:n.*35C>T
XM_011522187.2:c.1843C>T (PRC1)	XP_011520489.1:p.Pro615Ser
XM_011522188.3:c.1801C>T (PRC1)	XP_011520490.1:p.Pro601Ser
XM_011522189.2:c.1732C>T (PRC1)	XP_011520491.1:p.Pro578Ser
XM_011522190.3:c.1672C>T (PRC1)	XP_011520492.1:p.Pro558Ser
XM_011522191.3:c.*74C>T (PRC1)	XP_011520493.1:n.*74C>T
XM_011522192.2:c.1522C>T (PRC1)	XP_011520494.1:p.Pro508Ser
XM_017022712.2:c.*529C>T (PRC1)	XP_016878201.1:n.*529C>T
XM_017022713.2:c.*529C>T (PRC1)	XP_016878202.1:n.*529C>T
XM_017022714.2:c.1687C>T (PRC1)	XP_016878203.1:p.Pro563Ser
XM_017022715.2:c.*529C>T (PRC1)	XP_016878204.1:n.*529C>T
XM_017022716.2:c.*529C>T (PRC1)	XP_016878205.1:n.*529C>T
XM_017022717.1:c.*572C>T (PRC1)	XP_016878206.1:n.*572C>T
NM_003981.4:c.*529C>T (PRC1) MANE Select	NP_003972.2:n.*529C>T
NM_001267580.2:c.*572C>T (PRC1)	NP_001254509.2:n.*572C>T
NM_199413.3:c.*529C>T (PRC1)	NP_955445.2:n.*529C>T