Canonical Allele Identifier: CA492187778

Gene: PRC1 PRC1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.91509817T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966587T>G , CM000677.2:g.90966587T>G	GRCh38
NC_000015.9:g.91509817T>G , CM000677.1:g.91509817T>G	GRCh37
NC_000015.8:g.89310821T>G	NCBI36
NG_050647.1:g.33065A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*544A>C (PRC1) MANE Select	ENSP00000377793.3:n.*544A>C
ENST00000643536.1:c.*4169A>C	ENSP00000494429.1:n.*4169A>C
ENST00000361188.9:c.*544A>C (PRC1)	ENSP00000354679.5:n.*544A>C
ENST00000394249.7:c.*544A>C (PRC1)	ENSP00000377793.3:n.*544A>C
ENST00000555455.5:c.708A>C (PRC1)
ENST00000556972.6:c.191A>C (PRC1)	ENSP00000456737.1:n.191A>C
NM_001267580.1:c.*587A>C (PRC1)	NP_001254509.1:n.*587A>C
NM_003981.3:c.*544A>C (PRC1)	NP_003972.1:n.*544A>C
NM_199413.2:c.*544A>C (PRC1)	NP_955445.1:n.*544A>C
NR_051984.1:n.219T>G (PRC1-AS1)
XM_005254987.1:c.*587A>C (PRC1)	XP_005255044.1:n.*587A>C
XM_006720759.1:c.*638A>C (PRC1)	XP_006720822.1:n.*638A>C
XM_006720760.1:c.*50A>C (PRC1)	XP_006720823.1:n.*50A>C
XM_011522187.1:c.1858A>C (PRC1)	XP_011520489.1:p.Lys620Gln
XM_011522188.1:c.1816A>C (PRC1)	XP_011520490.1:p.Lys606Gln
XM_011522189.1:c.1747A>C (PRC1)	XP_011520491.1:p.Lys583Gln
XM_011522190.1:c.1687A>C (PRC1)	XP_011520492.1:p.Lys563Gln
XM_011522191.1:c.*89A>C (PRC1)	XP_011520493.1:n.*89A>C
XM_011522192.1:c.1537A>C (PRC1)	XP_011520494.1:p.Lys513Gln
XM_005254987.3:c.*587A>C (PRC1)	XP_005255044.1:n.*587A>C
XM_006720759.2:c.*638A>C (PRC1)	XP_006720822.1:n.*638A>C
XM_006720760.2:c.*50A>C (PRC1)	XP_006720823.1:n.*50A>C
XM_011522187.2:c.1858A>C (PRC1)	XP_011520489.1:p.Lys620Gln
XM_011522188.3:c.1816A>C (PRC1)	XP_011520490.1:p.Lys606Gln
XM_011522189.2:c.1747A>C (PRC1)	XP_011520491.1:p.Lys583Gln
XM_011522190.3:c.1687A>C (PRC1)	XP_011520492.1:p.Lys563Gln
XM_011522191.3:c.*89A>C (PRC1)	XP_011520493.1:n.*89A>C
XM_011522192.2:c.1537A>C (PRC1)	XP_011520494.1:p.Lys513Gln
XM_017022712.2:c.*544A>C (PRC1)	XP_016878201.1:n.*544A>C
XM_017022713.2:c.*544A>C (PRC1)	XP_016878202.1:n.*544A>C
XM_017022714.2:c.1702A>C (PRC1)	XP_016878203.1:p.Lys568Gln
XM_017022715.2:c.*544A>C (PRC1)	XP_016878204.1:n.*544A>C
XM_017022716.2:c.*544A>C (PRC1)	XP_016878205.1:n.*544A>C
XM_017022717.1:c.*587A>C (PRC1)	XP_016878206.1:n.*587A>C
NM_003981.4:c.*544A>C (PRC1) MANE Select	NP_003972.2:n.*544A>C
NM_001267580.2:c.*587A>C (PRC1)	NP_001254509.2:n.*587A>C
NM_199413.3:c.*544A>C (PRC1)	NP_955445.2:n.*544A>C