Canonical Allele Identifier: CA2195381187

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966361_90966362delinsAT , CM000677.2:g.90966361_90966362delinsAT	GRCh38
NC_000015.9:g.91509591_91509592delinsAT , CM000677.1:g.91509591_91509592delinsAT	GRCh37
NC_000015.8:g.89310595_89310596delinsAT	NCBI36
NG_050647.1:g.33290_33291delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000394249.8:c.*769_*770delinsAT MANE Select	ENSP00000377793.3:n.*769_*770delinsAT
ENST00000643536.1:c.*4394_*4395delinsAT	ENSP00000494429.1:n.*4394_*4395delinsAT
ENST00000361188.9:c.*769_*770delinsAT	ENSP00000354679.5:n.*769_*770delinsAT
ENST00000394249.7:c.*769_*770delinsAT	ENSP00000377793.3:n.*769_*770delinsAT
ENST00000556972.6:c.416_417delinsAT	ENSP00000456737.1:n.416_417delinsAT
NM_001267580.1:c.*812_*813delinsAT	NP_001254509.1:n.*812_*813delinsAT
NM_003981.3:c.*769_*770delinsAT	NP_003972.1:n.*769_*770delinsAT
NM_199413.2:c.*769_*770delinsAT	NP_955445.1:n.*769_*770delinsAT
XM_005254987.1:c.*812_*813delinsAT	XP_005255044.1:n.*812_*813delinsAT
XM_006720759.1:c.*863_*864delinsAT	XP_006720822.1:n.*863_*864delinsAT
XM_006720760.1:c.*275_*276delinsAT	XP_006720823.1:n.*275_*276delinsAT
XM_011522187.1:c.*217_*218delinsAT	XP_011520489.1:n.*217_*218delinsAT
XM_011522188.1:c.*217_*218delinsAT	XP_011520490.1:n.*217_*218delinsAT
XM_011522189.1:c.*217_*218delinsAT	XP_011520491.1:n.*217_*218delinsAT
XM_011522190.1:c.*217_*218delinsAT	XP_011520492.1:n.*217_*218delinsAT
XM_011522192.1:c.*217_*218delinsAT	XP_011520494.1:n.*217_*218delinsAT
XM_005254987.3:c.*812_*813delinsAT	XP_005255044.1:n.*812_*813delinsAT
XM_006720759.2:c.*863_*864delinsAT	XP_006720822.1:n.*863_*864delinsAT
XM_006720760.2:c.*275_*276delinsAT	XP_006720823.1:n.*275_*276delinsAT
XM_011522187.2:c.*217_*218delinsAT	XP_011520489.1:n.*217_*218delinsAT
XM_011522188.3:c.*217_*218delinsAT	XP_011520490.1:n.*217_*218delinsAT
XM_011522189.2:c.*217_*218delinsAT	XP_011520491.1:n.*217_*218delinsAT
XM_011522191.3:c.*314_*315delinsAT	XP_011520493.1:n.*314_*315delinsAT
XM_011522192.2:c.*217_*218delinsAT	XP_011520494.1:n.*217_*218delinsAT
XM_017022712.2:c.*769_*770delinsAT	XP_016878201.1:n.*769_*770delinsAT
XM_017022713.2:c.*769_*770delinsAT	XP_016878202.1:n.*769_*770delinsAT
XM_017022715.2:c.*769_*770delinsAT	XP_016878204.1:n.*769_*770delinsAT
XM_017022716.2:c.*769_*770delinsAT	XP_016878205.1:n.*769_*770delinsAT
XM_017022717.1:c.*812_*813delinsAT	XP_016878206.1:n.*812_*813delinsAT
NM_003981.4:c.*769_*770delinsAT MANE Select	NP_003972.2:n.*769_*770delinsAT
NM_001267580.2:c.*812_*813delinsAT	NP_001254509.2:n.*812_*813delinsAT
NM_199413.3:c.*769_*770delinsAT	NP_955445.2:n.*769_*770delinsAT