Canonical Allele Identifier: CA2195380992

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966208_90966212delinsACAGC , CM000677.2:g.90966208_90966212delinsACAGC	GRCh38
NC_000015.9:g.91509438_91509442delinsACAGC , CM000677.1:g.91509438_91509442delinsACAGC	GRCh37
NC_000015.8:g.89310442_89310446delinsACAGC	NCBI36
NG_050647.1:g.33440_33444delinsGCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*919_*923delinsGCTGT MANE Select	ENSP00000377793.3:n.*919_*923delinsGCTGT
ENST00000643536.1:c.*4544_*4548delinsGCTGT	ENSP00000494429.1:n.*4544_*4548delinsGCTGT
ENST00000361188.9:c.*919_*923delinsGCTGT	ENSP00000354679.5:n.*919_*923delinsGCTGT
ENST00000394249.7:c.*919_*923delinsGCTGT	ENSP00000377793.3:n.*919_*923delinsGCTGT
ENST00000556972.6:c.566_570delinsGCTGT	ENSP00000456737.1:n.566_570delinsGCTGT
NM_001267580.1:c.*962_*966delinsGCTGT	NP_001254509.1:n.*962_*966delinsGCTGT
NM_003981.3:c.*919_*923delinsGCTGT	NP_003972.1:n.*919_*923delinsGCTGT
NM_199413.2:c.*919_*923delinsGCTGT	NP_955445.1:n.*919_*923delinsGCTGT
XM_005254987.1:c.*962_*966delinsGCTGT	XP_005255044.1:n.*962_*966delinsGCTGT
XM_006720759.1:c.*1013_*1017delinsGCTGT	XP_006720822.1:n.*1013_*1017delinsGCTGT
XM_006720760.1:c.*425_*429delinsGCTGT	XP_006720823.1:n.*425_*429delinsGCTGT
XM_011522187.1:c.*367_*371delinsGCTGT	XP_011520489.1:n.*367_*371delinsGCTGT
XM_011522188.1:c.*367_*371delinsGCTGT	XP_011520490.1:n.*367_*371delinsGCTGT
XM_011522189.1:c.*367_*371delinsGCTGT	XP_011520491.1:n.*367_*371delinsGCTGT
XM_011522190.1:c.*367_*371delinsGCTGT	XP_011520492.1:n.*367_*371delinsGCTGT
XM_011522192.1:c.*367_*371delinsGCTGT	XP_011520494.1:n.*367_*371delinsGCTGT
XM_005254987.3:c.*962_*966delinsGCTGT	XP_005255044.1:n.*962_*966delinsGCTGT
XM_006720759.2:c.*1013_*1017delinsGCTGT	XP_006720822.1:n.*1013_*1017delinsGCTGT
XM_006720760.2:c.*425_*429delinsGCTGT	XP_006720823.1:n.*425_*429delinsGCTGT
XM_011522187.2:c.*367_*371delinsGCTGT	XP_011520489.1:n.*367_*371delinsGCTGT
XM_011522188.3:c.*367_*371delinsGCTGT	XP_011520490.1:n.*367_*371delinsGCTGT
XM_011522189.2:c.*367_*371delinsGCTGT	XP_011520491.1:n.*367_*371delinsGCTGT
XM_011522191.3:c.*464_*468delinsGCTGT	XP_011520493.1:n.*464_*468delinsGCTGT
XM_011522192.2:c.*367_*371delinsGCTGT	XP_011520494.1:n.*367_*371delinsGCTGT
XM_017022712.2:c.*919_*923delinsGCTGT	XP_016878201.1:n.*919_*923delinsGCTGT
XM_017022713.2:c.*919_*923delinsGCTGT	XP_016878202.1:n.*919_*923delinsGCTGT
XM_017022715.2:c.*919_*923delinsGCTGT	XP_016878204.1:n.*919_*923delinsGCTGT
XM_017022716.2:c.*919_*923delinsGCTGT	XP_016878205.1:n.*919_*923delinsGCTGT
XM_017022717.1:c.*962_*966delinsGCTGT	XP_016878206.1:n.*962_*966delinsGCTGT
NM_003981.4:c.*919_*923delinsGCTGT MANE Select	NP_003972.2:n.*919_*923delinsGCTGT
NM_001267580.2:c.*962_*966delinsGCTGT	NP_001254509.2:n.*962_*966delinsGCTGT
NM_199413.3:c.*919_*923delinsGCTGT	NP_955445.2:n.*919_*923delinsGCTGT