Canonical Allele Identifier: CA492187909

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs1567174774
• MyVariant Identifiers: chr15:g.91509859C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966629C>G , CM000677.2:g.90966629C>G	GRCh38
NC_000015.9:g.91509859C>G , CM000677.1:g.91509859C>G	GRCh37
NC_000015.8:g.89310863C>G	NCBI36
NG_050647.1:g.33023G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*502G>C (PRC1) MANE Select	ENSP00000377793.3:n.*502G>C
ENST00000643536.1:c.*4127G>C	ENSP00000494429.1:n.*4127G>C
ENST00000361188.9:c.*502G>C (PRC1)	ENSP00000354679.5:n.*502G>C
ENST00000394249.7:c.*502G>C (PRC1)	ENSP00000377793.3:n.*502G>C
ENST00000555455.5:c.666G>C (PRC1)
ENST00000556972.6:c.149G>C (PRC1)	ENSP00000456737.1:n.149G>C
NM_001267580.1:c.*545G>C (PRC1)	NP_001254509.1:n.*545G>C
NM_003981.3:c.*502G>C (PRC1)	NP_003972.1:n.*502G>C
NM_199413.2:c.*502G>C (PRC1)	NP_955445.1:n.*502G>C
NR_051984.1:n.261C>G (PRC1-AS1)
XM_005254987.1:c.*545G>C (PRC1)	XP_005255044.1:n.*545G>C
XM_006720759.1:c.*596G>C (PRC1)	XP_006720822.1:n.*596G>C
XM_006720760.1:c.*8G>C (PRC1)	XP_006720823.1:n.*8G>C
XM_011522187.1:c.1816G>C (PRC1)	XP_011520489.1:p.Val606Leu
XM_011522188.1:c.1774G>C (PRC1)	XP_011520490.1:p.Val592Leu
XM_011522189.1:c.1705G>C (PRC1)	XP_011520491.1:p.Val569Leu
XM_011522190.1:c.1645G>C (PRC1)	XP_011520492.1:p.Val549Leu
XM_011522191.1:c.*47G>C (PRC1)	XP_011520493.1:n.*47G>C
XM_011522192.1:c.1495G>C (PRC1)	XP_011520494.1:p.Val499Leu
XM_005254987.3:c.*545G>C (PRC1)	XP_005255044.1:n.*545G>C
XM_006720759.2:c.*596G>C (PRC1)	XP_006720822.1:n.*596G>C
XM_006720760.2:c.*8G>C (PRC1)	XP_006720823.1:n.*8G>C
XM_011522187.2:c.1816G>C (PRC1)	XP_011520489.1:p.Val606Leu
XM_011522188.3:c.1774G>C (PRC1)	XP_011520490.1:p.Val592Leu
XM_011522189.2:c.1705G>C (PRC1)	XP_011520491.1:p.Val569Leu
XM_011522190.3:c.1645G>C (PRC1)	XP_011520492.1:p.Val549Leu
XM_011522191.3:c.*47G>C (PRC1)	XP_011520493.1:n.*47G>C
XM_011522192.2:c.1495G>C (PRC1)	XP_011520494.1:p.Val499Leu
XM_017022712.2:c.*502G>C (PRC1)	XP_016878201.1:n.*502G>C
XM_017022713.2:c.*502G>C (PRC1)	XP_016878202.1:n.*502G>C
XM_017022714.2:c.1660G>C (PRC1)	XP_016878203.1:p.Val554Leu
XM_017022715.2:c.*502G>C (PRC1)	XP_016878204.1:n.*502G>C
XM_017022716.2:c.*502G>C (PRC1)	XP_016878205.1:n.*502G>C
XM_017022717.1:c.*545G>C (PRC1)	XP_016878206.1:n.*545G>C
NM_003981.4:c.*502G>C (PRC1) MANE Select	NP_003972.2:n.*502G>C
NM_001267580.2:c.*545G>C (PRC1)	NP_001254509.2:n.*545G>C
NM_199413.3:c.*502G>C (PRC1)	NP_955445.2:n.*502G>C