Canonical Allele Identifier: CA492187874

Gene: PRC1 PRC1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.91509849C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966619C>G , CM000677.2:g.90966619C>G	GRCh38
NC_000015.9:g.91509849C>G , CM000677.1:g.91509849C>G	GRCh37
NC_000015.8:g.89310853C>G	NCBI36
NG_050647.1:g.33033G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*512G>C (PRC1) MANE Select	ENSP00000377793.3:n.*512G>C
ENST00000643536.1:c.*4137G>C	ENSP00000494429.1:n.*4137G>C
ENST00000361188.9:c.*512G>C (PRC1)	ENSP00000354679.5:n.*512G>C
ENST00000394249.7:c.*512G>C (PRC1)	ENSP00000377793.3:n.*512G>C
ENST00000555455.5:c.676G>C (PRC1)
ENST00000556972.6:c.159G>C (PRC1)	ENSP00000456737.1:n.159G>C
NM_001267580.1:c.*555G>C (PRC1)	NP_001254509.1:n.*555G>C
NM_003981.3:c.*512G>C (PRC1)	NP_003972.1:n.*512G>C
NM_199413.2:c.*512G>C (PRC1)	NP_955445.1:n.*512G>C
NR_051984.1:n.251C>G (PRC1-AS1)
XM_005254987.1:c.*555G>C (PRC1)	XP_005255044.1:n.*555G>C
XM_006720759.1:c.*606G>C (PRC1)	XP_006720822.1:n.*606G>C
XM_006720760.1:c.*18G>C (PRC1)	XP_006720823.1:n.*18G>C
XM_011522187.1:c.1826G>C (PRC1)	XP_011520489.1:p.Cys609Ser
XM_011522188.1:c.1784G>C (PRC1)	XP_011520490.1:p.Cys595Ser
XM_011522189.1:c.1715G>C (PRC1)	XP_011520491.1:p.Cys572Ser
XM_011522190.1:c.1655G>C (PRC1)	XP_011520492.1:p.Cys552Ser
XM_011522191.1:c.*57G>C (PRC1)	XP_011520493.1:n.*57G>C
XM_011522192.1:c.1505G>C (PRC1)	XP_011520494.1:p.Cys502Ser
XM_005254987.3:c.*555G>C (PRC1)	XP_005255044.1:n.*555G>C
XM_006720759.2:c.*606G>C (PRC1)	XP_006720822.1:n.*606G>C
XM_006720760.2:c.*18G>C (PRC1)	XP_006720823.1:n.*18G>C
XM_011522187.2:c.1826G>C (PRC1)	XP_011520489.1:p.Cys609Ser
XM_011522188.3:c.1784G>C (PRC1)	XP_011520490.1:p.Cys595Ser
XM_011522189.2:c.1715G>C (PRC1)	XP_011520491.1:p.Cys572Ser
XM_011522190.3:c.1655G>C (PRC1)	XP_011520492.1:p.Cys552Ser
XM_011522191.3:c.*57G>C (PRC1)	XP_011520493.1:n.*57G>C
XM_011522192.2:c.1505G>C (PRC1)	XP_011520494.1:p.Cys502Ser
XM_017022712.2:c.*512G>C (PRC1)	XP_016878201.1:n.*512G>C
XM_017022713.2:c.*512G>C (PRC1)	XP_016878202.1:n.*512G>C
XM_017022714.2:c.1670G>C (PRC1)	XP_016878203.1:p.Cys557Ser
XM_017022715.2:c.*512G>C (PRC1)	XP_016878204.1:n.*512G>C
XM_017022716.2:c.*512G>C (PRC1)	XP_016878205.1:n.*512G>C
XM_017022717.1:c.*555G>C (PRC1)	XP_016878206.1:n.*555G>C
NM_003981.4:c.*512G>C (PRC1) MANE Select	NP_003972.2:n.*512G>C
NM_001267580.2:c.*555G>C (PRC1)	NP_001254509.2:n.*555G>C
NM_199413.3:c.*512G>C (PRC1)	NP_955445.2:n.*512G>C