Canonical Allele Identifier: CA492187882

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs2037510562
• MyVariant Identifiers: chr15:g.91509851C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966621C>G , CM000677.2:g.90966621C>G	GRCh38
NC_000015.9:g.91509851C>G , CM000677.1:g.91509851C>G	GRCh37
NC_000015.8:g.89310855C>G	NCBI36
NG_050647.1:g.33031G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*510G>C (PRC1) MANE Select	ENSP00000377793.3:n.*510G>C
ENST00000643536.1:c.*4135G>C	ENSP00000494429.1:n.*4135G>C
ENST00000361188.9:c.*510G>C (PRC1)	ENSP00000354679.5:n.*510G>C
ENST00000394249.7:c.*510G>C (PRC1)	ENSP00000377793.3:n.*510G>C
ENST00000555455.5:c.674G>C (PRC1)
ENST00000556972.6:c.157G>C (PRC1)	ENSP00000456737.1:n.157G>C
NM_001267580.1:c.*553G>C (PRC1)	NP_001254509.1:n.*553G>C
NM_003981.3:c.*510G>C (PRC1)	NP_003972.1:n.*510G>C
NM_199413.2:c.*510G>C (PRC1)	NP_955445.1:n.*510G>C
NR_051984.1:n.253C>G (PRC1-AS1)
XM_005254987.1:c.*553G>C (PRC1)	XP_005255044.1:n.*553G>C
XM_006720759.1:c.*604G>C (PRC1)	XP_006720822.1:n.*604G>C
XM_006720760.1:c.*16G>C (PRC1)	XP_006720823.1:n.*16G>C
XM_011522187.1:c.1824G>C (PRC1)	XP_011520489.1:p.Val608=
XM_011522188.1:c.1782G>C (PRC1)	XP_011520490.1:p.Val594=
XM_011522189.1:c.1713G>C (PRC1)	XP_011520491.1:p.Val571=
XM_011522190.1:c.1653G>C (PRC1)	XP_011520492.1:p.Val551=
XM_011522191.1:c.*55G>C (PRC1)	XP_011520493.1:n.*55G>C
XM_011522192.1:c.1503G>C (PRC1)	XP_011520494.1:p.Val501=
XM_005254987.3:c.*553G>C (PRC1)	XP_005255044.1:n.*553G>C
XM_006720759.2:c.*604G>C (PRC1)	XP_006720822.1:n.*604G>C
XM_006720760.2:c.*16G>C (PRC1)	XP_006720823.1:n.*16G>C
XM_011522187.2:c.1824G>C (PRC1)	XP_011520489.1:p.Val608=
XM_011522188.3:c.1782G>C (PRC1)	XP_011520490.1:p.Val594=
XM_011522189.2:c.1713G>C (PRC1)	XP_011520491.1:p.Val571=
XM_011522190.3:c.1653G>C (PRC1)	XP_011520492.1:p.Val551=
XM_011522191.3:c.*55G>C (PRC1)	XP_011520493.1:n.*55G>C
XM_011522192.2:c.1503G>C (PRC1)	XP_011520494.1:p.Val501=
XM_017022712.2:c.*510G>C (PRC1)	XP_016878201.1:n.*510G>C
XM_017022713.2:c.*510G>C (PRC1)	XP_016878202.1:n.*510G>C
XM_017022714.2:c.1668G>C (PRC1)	XP_016878203.1:p.Val556=
XM_017022715.2:c.*510G>C (PRC1)	XP_016878204.1:n.*510G>C
XM_017022716.2:c.*510G>C (PRC1)	XP_016878205.1:n.*510G>C
XM_017022717.1:c.*553G>C (PRC1)	XP_016878206.1:n.*553G>C
NM_003981.4:c.*510G>C (PRC1) MANE Select	NP_003972.2:n.*510G>C
NM_001267580.2:c.*553G>C (PRC1)	NP_001254509.2:n.*553G>C
NM_199413.3:c.*510G>C (PRC1)	NP_955445.2:n.*510G>C