Canonical Allele Identifier: CA393870644

Gene: PRC1 PRC1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.91509868C>A (hg19) ; chr15:g.90966638C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966638C>A , CM000677.2:g.90966638C>A	GRCh38
NC_000015.9:g.91509868C>A , CM000677.1:g.91509868C>A	GRCh37
NC_000015.8:g.89310872C>A	NCBI36
NG_050647.1:g.33014G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*493G>T (PRC1) MANE Select	ENSP00000377793.3:n.*493G>T
ENST00000643536.1:c.*4118G>T	ENSP00000494429.1:n.*4118G>T
ENST00000361188.9:c.*493G>T (PRC1)	ENSP00000354679.5:n.*493G>T
ENST00000394249.7:c.*493G>T (PRC1)	ENSP00000377793.3:n.*493G>T
ENST00000555455.5:c.657G>T (PRC1)
ENST00000556972.6:c.140G>T (PRC1)	ENSP00000456737.1:p.Ter47Leu
NM_001267580.1:c.*536G>T (PRC1)	NP_001254509.1:n.*536G>T
NM_003981.3:c.*493G>T (PRC1)	NP_003972.1:n.*493G>T
NM_199413.2:c.*493G>T (PRC1)	NP_955445.1:n.*493G>T
NR_051984.1:n.270C>A (PRC1-AS1)
XM_005254987.1:c.*536G>T (PRC1)	XP_005255044.1:n.*536G>T
XM_006720759.1:c.*587G>T (PRC1)	XP_006720822.1:n.*587G>T
XM_006720760.1:c.1688G>T (PRC1)	XP_006720823.1:p.Ter563Leu
XM_011522187.1:c.1807G>T (PRC1)	XP_011520489.1:p.Glu603Ter
XM_011522188.1:c.1765G>T (PRC1)	XP_011520490.1:p.Glu589Ter
XM_011522189.1:c.1696G>T (PRC1)	XP_011520491.1:p.Glu566Ter
XM_011522190.1:c.1636G>T (PRC1)	XP_011520492.1:p.Glu546Ter
XM_011522191.1:c.*38G>T (PRC1)	XP_011520493.1:n.*38G>T
XM_011522192.1:c.1486G>T (PRC1)	XP_011520494.1:p.Glu496Ter
XM_005254987.3:c.*536G>T (PRC1)	XP_005255044.1:n.*536G>T
XM_006720759.2:c.*587G>T (PRC1)	XP_006720822.1:n.*587G>T
XM_006720760.2:c.1688G>T (PRC1)	XP_006720823.1:p.Ter563Leu
XM_011522187.2:c.1807G>T (PRC1)	XP_011520489.1:p.Glu603Ter
XM_011522188.3:c.1765G>T (PRC1)	XP_011520490.1:p.Glu589Ter
XM_011522189.2:c.1696G>T (PRC1)	XP_011520491.1:p.Glu566Ter
XM_011522190.3:c.1636G>T (PRC1)	XP_011520492.1:p.Glu546Ter
XM_011522191.3:c.*38G>T (PRC1)	XP_011520493.1:n.*38G>T
XM_011522192.2:c.1486G>T (PRC1)	XP_011520494.1:p.Glu496Ter
XM_017022712.2:c.*493G>T (PRC1)	XP_016878201.1:n.*493G>T
XM_017022713.2:c.*493G>T (PRC1)	XP_016878202.1:n.*493G>T
XM_017022714.2:c.1651G>T (PRC1)	XP_016878203.1:p.Glu551Ter
XM_017022715.2:c.*493G>T (PRC1)	XP_016878204.1:n.*493G>T
XM_017022716.2:c.*493G>T (PRC1)	XP_016878205.1:n.*493G>T
XM_017022717.1:c.*536G>T (PRC1)	XP_016878206.1:n.*536G>T
NM_003981.4:c.*493G>T (PRC1) MANE Select	NP_003972.2:n.*493G>T
NM_001267580.2:c.*536G>T (PRC1)	NP_001254509.2:n.*536G>T
NM_199413.3:c.*493G>T (PRC1)	NP_955445.2:n.*493G>T