Canonical Allele Identifier: CA2520286486

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966248_90966249insTGGTG , CM000677.2:g.90966248_90966249insTGGTG	GRCh38
NC_000015.9:g.91509478_91509479insTGGTG , CM000677.1:g.91509478_91509479insTGGTG	GRCh37
NC_000015.8:g.89310482_89310483insTGGTG	NCBI36
NG_050647.1:g.33406_33407insCACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*885_*886insCACAC MANE Select	ENSP00000377793.3:n.*885_*886insCACAC
ENST00000643536.1:c.*4510_*4511insCACAC	ENSP00000494429.1:n.*4510_*4511insCACAC
ENST00000361188.9:c.*885_*886insCACAC	ENSP00000354679.5:n.*885_*886insCACAC
ENST00000394249.7:c.*885_*886insCACAC	ENSP00000377793.3:n.*885_*886insCACAC
ENST00000556972.6:c.532_533insCACAC	ENSP00000456737.1:n.532_533insCACAC
NM_001267580.1:c.*928_*929insCACAC	NP_001254509.1:n.*928_*929insCACAC
NM_003981.3:c.*885_*886insCACAC	NP_003972.1:n.*885_*886insCACAC
NM_199413.2:c.*885_*886insCACAC	NP_955445.1:n.*885_*886insCACAC
XM_005254987.1:c.*928_*929insCACAC	XP_005255044.1:n.*928_*929insCACAC
XM_006720759.1:c.*979_*980insCACAC	XP_006720822.1:n.*979_*980insCACAC
XM_006720760.1:c.*391_*392insCACAC	XP_006720823.1:n.*391_*392insCACAC
XM_011522187.1:c.*333_*334insCACAC	XP_011520489.1:n.*333_*334insCACAC
XM_011522188.1:c.*333_*334insCACAC	XP_011520490.1:n.*333_*334insCACAC
XM_011522189.1:c.*333_*334insCACAC	XP_011520491.1:n.*333_*334insCACAC
XM_011522190.1:c.*333_*334insCACAC	XP_011520492.1:n.*333_*334insCACAC
XM_011522192.1:c.*333_*334insCACAC	XP_011520494.1:n.*333_*334insCACAC
XM_005254987.3:c.*928_*929insCACAC	XP_005255044.1:n.*928_*929insCACAC
XM_006720759.2:c.*979_*980insCACAC	XP_006720822.1:n.*979_*980insCACAC
XM_006720760.2:c.*391_*392insCACAC	XP_006720823.1:n.*391_*392insCACAC
XM_011522187.2:c.*333_*334insCACAC	XP_011520489.1:n.*333_*334insCACAC
XM_011522188.3:c.*333_*334insCACAC	XP_011520490.1:n.*333_*334insCACAC
XM_011522189.2:c.*333_*334insCACAC	XP_011520491.1:n.*333_*334insCACAC
XM_011522191.3:c.*430_*431insCACAC	XP_011520493.1:n.*430_*431insCACAC
XM_011522192.2:c.*333_*334insCACAC	XP_011520494.1:n.*333_*334insCACAC
XM_017022712.2:c.*885_*886insCACAC	XP_016878201.1:n.*885_*886insCACAC
XM_017022713.2:c.*885_*886insCACAC	XP_016878202.1:n.*885_*886insCACAC
XM_017022715.2:c.*885_*886insCACAC	XP_016878204.1:n.*885_*886insCACAC
XM_017022716.2:c.*885_*886insCACAC	XP_016878205.1:n.*885_*886insCACAC
XM_017022717.1:c.*928_*929insCACAC	XP_016878206.1:n.*928_*929insCACAC
NM_003981.4:c.*885_*886insCACAC MANE Select	NP_003972.2:n.*885_*886insCACAC
NM_001267580.2:c.*928_*929insCACAC	NP_001254509.2:n.*928_*929insCACAC
NM_199413.3:c.*885_*886insCACAC	NP_955445.2:n.*885_*886insCACAC