Canonical Allele Identifier: CA2195381024

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966221_90966224delinsAAAT , CM000677.2:g.90966221_90966224delinsAAAT	GRCh38
NC_000015.9:g.91509451_91509454delinsAAAT , CM000677.1:g.91509451_91509454delinsAAAT	GRCh37
NC_000015.8:g.89310455_89310458delinsAAAT	NCBI36
NG_050647.1:g.33428_33431delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*907_*910delinsATTT MANE Select	ENSP00000377793.3:n.*907_*910delinsATTT
ENST00000643536.1:c.*4532_*4535delinsATTT	ENSP00000494429.1:n.*4532_*4535delinsATTT
ENST00000361188.9:c.*907_*910delinsATTT	ENSP00000354679.5:n.*907_*910delinsATTT
ENST00000394249.7:c.*907_*910delinsATTT	ENSP00000377793.3:n.*907_*910delinsATTT
ENST00000556972.6:c.554_557delinsATTT	ENSP00000456737.1:n.554_557delinsATTT
NM_001267580.1:c.*950_*953delinsATTT	NP_001254509.1:n.*950_*953delinsATTT
NM_003981.3:c.*907_*910delinsATTT	NP_003972.1:n.*907_*910delinsATTT
NM_199413.2:c.*907_*910delinsATTT	NP_955445.1:n.*907_*910delinsATTT
XM_005254987.1:c.*950_*953delinsATTT	XP_005255044.1:n.*950_*953delinsATTT
XM_006720759.1:c.*1001_*1004delinsATTT	XP_006720822.1:n.*1001_*1004delinsATTT
XM_006720760.1:c.*413_*416delinsATTT	XP_006720823.1:n.*413_*416delinsATTT
XM_011522187.1:c.*355_*358delinsATTT	XP_011520489.1:n.*355_*358delinsATTT
XM_011522188.1:c.*355_*358delinsATTT	XP_011520490.1:n.*355_*358delinsATTT
XM_011522189.1:c.*355_*358delinsATTT	XP_011520491.1:n.*355_*358delinsATTT
XM_011522190.1:c.*355_*358delinsATTT	XP_011520492.1:n.*355_*358delinsATTT
XM_011522192.1:c.*355_*358delinsATTT	XP_011520494.1:n.*355_*358delinsATTT
XM_005254987.3:c.*950_*953delinsATTT	XP_005255044.1:n.*950_*953delinsATTT
XM_006720759.2:c.*1001_*1004delinsATTT	XP_006720822.1:n.*1001_*1004delinsATTT
XM_006720760.2:c.*413_*416delinsATTT	XP_006720823.1:n.*413_*416delinsATTT
XM_011522187.2:c.*355_*358delinsATTT	XP_011520489.1:n.*355_*358delinsATTT
XM_011522188.3:c.*355_*358delinsATTT	XP_011520490.1:n.*355_*358delinsATTT
XM_011522189.2:c.*355_*358delinsATTT	XP_011520491.1:n.*355_*358delinsATTT
XM_011522191.3:c.*452_*455delinsATTT	XP_011520493.1:n.*452_*455delinsATTT
XM_011522192.2:c.*355_*358delinsATTT	XP_011520494.1:n.*355_*358delinsATTT
XM_017022712.2:c.*907_*910delinsATTT	XP_016878201.1:n.*907_*910delinsATTT
XM_017022713.2:c.*907_*910delinsATTT	XP_016878202.1:n.*907_*910delinsATTT
XM_017022715.2:c.*907_*910delinsATTT	XP_016878204.1:n.*907_*910delinsATTT
XM_017022716.2:c.*907_*910delinsATTT	XP_016878205.1:n.*907_*910delinsATTT
XM_017022717.1:c.*950_*953delinsATTT	XP_016878206.1:n.*950_*953delinsATTT
NM_003981.4:c.*907_*910delinsATTT MANE Select	NP_003972.2:n.*907_*910delinsATTT
NM_001267580.2:c.*950_*953delinsATTT	NP_001254509.2:n.*950_*953delinsATTT
NM_199413.3:c.*907_*910delinsATTT	NP_955445.2:n.*907_*910delinsATTT