Canonical Allele Identifier: CA492187428

Gene: PRC1 PRC1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.91509702G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966472G>T , CM000677.2:g.90966472G>T	GRCh38
NC_000015.9:g.91509702G>T , CM000677.1:g.91509702G>T	GRCh37
NC_000015.8:g.89310706G>T	NCBI36
NG_050647.1:g.33180C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*659C>A (PRC1) MANE Select	ENSP00000377793.3:n.*659C>A
ENST00000643536.1:c.*4284C>A	ENSP00000494429.1:n.*4284C>A
ENST00000361188.9:c.*659C>A (PRC1)	ENSP00000354679.5:n.*659C>A
ENST00000394249.7:c.*659C>A (PRC1)	ENSP00000377793.3:n.*659C>A
ENST00000555455.5:c.823C>A (PRC1)
ENST00000556972.6:c.306C>A (PRC1)	ENSP00000456737.1:n.306C>A
NM_001267580.1:c.*702C>A (PRC1)	NP_001254509.1:n.*702C>A
NM_003981.3:c.*659C>A (PRC1)	NP_003972.1:n.*659C>A
NM_199413.2:c.*659C>A (PRC1)	NP_955445.1:n.*659C>A
NR_051984.1:n.104G>T (PRC1-AS1)
XM_005254987.1:c.*702C>A (PRC1)	XP_005255044.1:n.*702C>A
XM_006720759.1:c.*753C>A (PRC1)	XP_006720822.1:n.*753C>A
XM_006720760.1:c.*165C>A (PRC1)	XP_006720823.1:n.*165C>A
XM_011522187.1:c.*107C>A (PRC1)	XP_011520489.1:n.*107C>A
XM_011522188.1:c.*107C>A (PRC1)	XP_011520490.1:n.*107C>A
XM_011522189.1:c.*107C>A (PRC1)	XP_011520491.1:n.*107C>A
XM_011522190.1:c.*107C>A (PRC1)	XP_011520492.1:n.*107C>A
XM_011522192.1:c.*107C>A (PRC1)	XP_011520494.1:n.*107C>A
XM_005254987.3:c.*702C>A (PRC1)	XP_005255044.1:n.*702C>A
XM_006720759.2:c.*753C>A (PRC1)	XP_006720822.1:n.*753C>A
XM_006720760.2:c.*165C>A (PRC1)	XP_006720823.1:n.*165C>A
XM_011522187.2:c.*107C>A (PRC1)	XP_011520489.1:n.*107C>A
XM_011522188.3:c.*107C>A (PRC1)	XP_011520490.1:n.*107C>A
XM_011522189.2:c.*107C>A (PRC1)	XP_011520491.1:n.*107C>A
XM_011522191.3:c.*204C>A (PRC1)	XP_011520493.1:n.*204C>A
XM_011522192.2:c.*107C>A (PRC1)	XP_011520494.1:n.*107C>A
XM_017022712.2:c.*659C>A (PRC1)	XP_016878201.1:n.*659C>A
XM_017022713.2:c.*659C>A (PRC1)	XP_016878202.1:n.*659C>A
XM_017022715.2:c.*659C>A (PRC1)	XP_016878204.1:n.*659C>A
XM_017022716.2:c.*659C>A (PRC1)	XP_016878205.1:n.*659C>A
XM_017022717.1:c.*702C>A (PRC1)	XP_016878206.1:n.*702C>A
NM_003981.4:c.*659C>A (PRC1) MANE Select	NP_003972.2:n.*659C>A
NM_001267580.2:c.*702C>A (PRC1)	NP_001254509.2:n.*702C>A
NM_199413.3:c.*659C>A (PRC1)	NP_955445.2:n.*659C>A