Canonical Allele Identifier: CA2195380996

Gene: PRC1

Linked Data

• dbSNP Id: rs2037474286

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966209_90966212del , CM000677.2:g.90966209_90966212del	GRCh38
NC_000015.9:g.91509439_91509442del , CM000677.1:g.91509439_91509442del	GRCh37
NC_000015.8:g.89310443_89310446del	NCBI36
NG_050647.1:g.33440_33443del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*919_*922del MANE Select	ENSP00000377793.3:n.*919_*922del
ENST00000643536.1:c.*4544_*4547del	ENSP00000494429.1:n.*4544_*4547del
ENST00000361188.9:c.*919_*922del	ENSP00000354679.5:n.*919_*922del
ENST00000394249.7:c.*919_*922del	ENSP00000377793.3:n.*919_*922del
ENST00000556972.6:c.566_569del	ENSP00000456737.1:n.566_569del
NM_001267580.1:c.*962_*965del	NP_001254509.1:n.*962_*965del
NM_003981.3:c.*919_*922del	NP_003972.1:n.*919_*922del
NM_199413.2:c.*919_*922del	NP_955445.1:n.*919_*922del
XM_005254987.1:c.*962_*965del	XP_005255044.1:n.*962_*965del
XM_006720759.1:c.*1013_*1016del	XP_006720822.1:n.*1013_*1016del
XM_006720760.1:c.*425_*428del	XP_006720823.1:n.*425_*428del
XM_011522187.1:c.*367_*370del	XP_011520489.1:n.*367_*370del
XM_011522188.1:c.*367_*370del	XP_011520490.1:n.*367_*370del
XM_011522189.1:c.*367_*370del	XP_011520491.1:n.*367_*370del
XM_011522190.1:c.*367_*370del	XP_011520492.1:n.*367_*370del
XM_011522192.1:c.*367_*370del	XP_011520494.1:n.*367_*370del
XM_005254987.3:c.*962_*965del	XP_005255044.1:n.*962_*965del
XM_006720759.2:c.*1013_*1016del	XP_006720822.1:n.*1013_*1016del
XM_006720760.2:c.*425_*428del	XP_006720823.1:n.*425_*428del
XM_011522187.2:c.*367_*370del	XP_011520489.1:n.*367_*370del
XM_011522188.3:c.*367_*370del	XP_011520490.1:n.*367_*370del
XM_011522189.2:c.*367_*370del	XP_011520491.1:n.*367_*370del
XM_011522191.3:c.*464_*467del	XP_011520493.1:n.*464_*467del
XM_011522192.2:c.*367_*370del	XP_011520494.1:n.*367_*370del
XM_017022712.2:c.*919_*922del	XP_016878201.1:n.*919_*922del
XM_017022713.2:c.*919_*922del	XP_016878202.1:n.*919_*922del
XM_017022715.2:c.*919_*922del	XP_016878204.1:n.*919_*922del
XM_017022716.2:c.*919_*922del	XP_016878205.1:n.*919_*922del
XM_017022717.1:c.*962_*965del	XP_016878206.1:n.*962_*965del
NM_003981.4:c.*919_*922del MANE Select	NP_003972.2:n.*919_*922del
NM_001267580.2:c.*962_*965del	NP_001254509.2:n.*962_*965del
NM_199413.3:c.*919_*922del	NP_955445.2:n.*919_*922del