Canonical Allele Identifier: CA492187943

Gene: PRC1 PRC1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.91509882T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966652T>A , CM000677.2:g.90966652T>A	GRCh38
NC_000015.9:g.91509882T>A , CM000677.1:g.91509882T>A	GRCh37
NC_000015.8:g.89310886T>A	NCBI36
NG_050647.1:g.33000A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*479A>T (PRC1) MANE Select	ENSP00000377793.3:n.*479A>T
ENST00000643536.1:c.*4104A>T	ENSP00000494429.1:n.*4104A>T
ENST00000361188.9:c.*479A>T (PRC1)	ENSP00000354679.5:n.*479A>T
ENST00000394249.7:c.*479A>T (PRC1)	ENSP00000377793.3:n.*479A>T
ENST00000555455.5:c.643A>T (PRC1)
ENST00000556972.6:c.126A>T (PRC1)	ENSP00000456737.1:p.Gly42=
NM_001267580.1:c.*522A>T (PRC1)	NP_001254509.1:n.*522A>T
NM_003981.3:c.*479A>T (PRC1)	NP_003972.1:n.*479A>T
NM_199413.2:c.*479A>T (PRC1)	NP_955445.1:n.*479A>T
NR_051984.1:n.284T>A (PRC1-AS1)
XM_005254987.1:c.*522A>T (PRC1)	XP_005255044.1:n.*522A>T
XM_006720759.1:c.*573A>T (PRC1)	XP_006720822.1:n.*573A>T
XM_006720760.1:c.1674A>T (PRC1)	XP_006720823.1:p.Gly558=
XM_011522187.1:c.1793A>T (PRC1)	XP_011520489.1:p.Asp598Val
XM_011522188.1:c.1751A>T (PRC1)	XP_011520490.1:p.Asp584Val
XM_011522189.1:c.1682A>T (PRC1)	XP_011520491.1:p.Asp561Val
XM_011522190.1:c.1622A>T (PRC1)	XP_011520492.1:p.Asp541Val
XM_011522191.1:c.*24A>T (PRC1)	XP_011520493.1:n.*24A>T
XM_011522192.1:c.1472A>T (PRC1)	XP_011520494.1:p.Asp491Val
XM_005254987.3:c.*522A>T (PRC1)	XP_005255044.1:n.*522A>T
XM_006720759.2:c.*573A>T (PRC1)	XP_006720822.1:n.*573A>T
XM_006720760.2:c.1674A>T (PRC1)	XP_006720823.1:p.Gly558=
XM_011522187.2:c.1793A>T (PRC1)	XP_011520489.1:p.Asp598Val
XM_011522188.3:c.1751A>T (PRC1)	XP_011520490.1:p.Asp584Val
XM_011522189.2:c.1682A>T (PRC1)	XP_011520491.1:p.Asp561Val
XM_011522190.3:c.1622A>T (PRC1)	XP_011520492.1:p.Asp541Val
XM_011522191.3:c.*24A>T (PRC1)	XP_011520493.1:n.*24A>T
XM_011522192.2:c.1472A>T (PRC1)	XP_011520494.1:p.Asp491Val
XM_017022712.2:c.*479A>T (PRC1)	XP_016878201.1:n.*479A>T
XM_017022713.2:c.*479A>T (PRC1)	XP_016878202.1:n.*479A>T
XM_017022714.2:c.1637A>T (PRC1)	XP_016878203.1:p.Asp546Val
XM_017022715.2:c.*479A>T (PRC1)	XP_016878204.1:n.*479A>T
XM_017022716.2:c.*479A>T (PRC1)	XP_016878205.1:n.*479A>T
XM_017022717.1:c.*522A>T (PRC1)	XP_016878206.1:n.*522A>T
NM_003981.4:c.*479A>T (PRC1) MANE Select	NP_003972.2:n.*479A>T
NM_001267580.2:c.*522A>T (PRC1)	NP_001254509.2:n.*522A>T
NM_199413.3:c.*479A>T (PRC1)	NP_955445.2:n.*479A>T