Canonical Allele Identifier: CA492187175

Gene: PRC1 PRC1-AS1

Linked Data

• MyVariant Identifiers: chr15:g.91509614G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966384G>A , CM000677.2:g.90966384G>A	GRCh38
NC_000015.9:g.91509614G>A , CM000677.1:g.91509614G>A	GRCh37
NC_000015.8:g.89310618G>A	NCBI36
NG_050647.1:g.33268C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*747C>T (PRC1) MANE Select	ENSP00000377793.3:n.*747C>T
ENST00000643536.1:c.*4372C>T	ENSP00000494429.1:n.*4372C>T
ENST00000361188.9:c.*747C>T (PRC1)	ENSP00000354679.5:n.*747C>T
ENST00000394249.7:c.*747C>T (PRC1)	ENSP00000377793.3:n.*747C>T
ENST00000556972.6:c.394C>T (PRC1)	ENSP00000456737.1:n.394C>T
NM_001267580.1:c.*790C>T (PRC1)	NP_001254509.1:n.*790C>T
NM_003981.3:c.*747C>T (PRC1)	NP_003972.1:n.*747C>T
NM_199413.2:c.*747C>T (PRC1)	NP_955445.1:n.*747C>T
NR_051984.1:n.16G>A (PRC1-AS1)
XM_005254987.1:c.*790C>T (PRC1)	XP_005255044.1:n.*790C>T
XM_006720759.1:c.*841C>T (PRC1)	XP_006720822.1:n.*841C>T
XM_006720760.1:c.*253C>T (PRC1)	XP_006720823.1:n.*253C>T
XM_011522187.1:c.*195C>T (PRC1)	XP_011520489.1:n.*195C>T
XM_011522188.1:c.*195C>T (PRC1)	XP_011520490.1:n.*195C>T
XM_011522189.1:c.*195C>T (PRC1)	XP_011520491.1:n.*195C>T
XM_011522190.1:c.*195C>T (PRC1)	XP_011520492.1:n.*195C>T
XM_011522192.1:c.*195C>T (PRC1)	XP_011520494.1:n.*195C>T
XM_005254987.3:c.*790C>T (PRC1)	XP_005255044.1:n.*790C>T
XM_006720759.2:c.*841C>T (PRC1)	XP_006720822.1:n.*841C>T
XM_006720760.2:c.*253C>T (PRC1)	XP_006720823.1:n.*253C>T
XM_011522187.2:c.*195C>T (PRC1)	XP_011520489.1:n.*195C>T
XM_011522188.3:c.*195C>T (PRC1)	XP_011520490.1:n.*195C>T
XM_011522189.2:c.*195C>T (PRC1)	XP_011520491.1:n.*195C>T
XM_011522191.3:c.*292C>T (PRC1)	XP_011520493.1:n.*292C>T
XM_011522192.2:c.*195C>T (PRC1)	XP_011520494.1:n.*195C>T
XM_017022712.2:c.*747C>T (PRC1)	XP_016878201.1:n.*747C>T
XM_017022713.2:c.*747C>T (PRC1)	XP_016878202.1:n.*747C>T
XM_017022715.2:c.*747C>T (PRC1)	XP_016878204.1:n.*747C>T
XM_017022716.2:c.*747C>T (PRC1)	XP_016878205.1:n.*747C>T
XM_017022717.1:c.*790C>T (PRC1)	XP_016878206.1:n.*790C>T
NM_003981.4:c.*747C>T (PRC1) MANE Select	NP_003972.2:n.*747C>T
NM_001267580.2:c.*790C>T (PRC1)	NP_001254509.2:n.*790C>T
NM_199413.3:c.*747C>T (PRC1)	NP_955445.2:n.*747C>T