Canonical Allele Identifier: CA2195381016

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966217_90966221delinsGAATA , CM000677.2:g.90966217_90966221delinsGAATA	GRCh38
NC_000015.9:g.91509447_91509451delinsGAATA , CM000677.1:g.91509447_91509451delinsGAATA	GRCh37
NC_000015.8:g.89310451_89310455delinsGAATA	NCBI36
NG_050647.1:g.33431_33435delinsTATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*910_*914delinsTATTC MANE Select	ENSP00000377793.3:n.*910_*914delinsTATTC
ENST00000643536.1:c.*4535_*4539delinsTATTC	ENSP00000494429.1:n.*4535_*4539delinsTATTC
ENST00000361188.9:c.*910_*914delinsTATTC	ENSP00000354679.5:n.*910_*914delinsTATTC
ENST00000394249.7:c.*910_*914delinsTATTC	ENSP00000377793.3:n.*910_*914delinsTATTC
ENST00000556972.6:c.557_561delinsTATTC	ENSP00000456737.1:n.557_561delinsTATTC
NM_001267580.1:c.*953_*957delinsTATTC	NP_001254509.1:n.*953_*957delinsTATTC
NM_003981.3:c.*910_*914delinsTATTC	NP_003972.1:n.*910_*914delinsTATTC
NM_199413.2:c.*910_*914delinsTATTC	NP_955445.1:n.*910_*914delinsTATTC
XM_005254987.1:c.*953_*957delinsTATTC	XP_005255044.1:n.*953_*957delinsTATTC
XM_006720759.1:c.*1004_*1008delinsTATTC	XP_006720822.1:n.*1004_*1008delinsTATTC
XM_006720760.1:c.*416_*420delinsTATTC	XP_006720823.1:n.*416_*420delinsTATTC
XM_011522187.1:c.*358_*362delinsTATTC	XP_011520489.1:n.*358_*362delinsTATTC
XM_011522188.1:c.*358_*362delinsTATTC	XP_011520490.1:n.*358_*362delinsTATTC
XM_011522189.1:c.*358_*362delinsTATTC	XP_011520491.1:n.*358_*362delinsTATTC
XM_011522190.1:c.*358_*362delinsTATTC	XP_011520492.1:n.*358_*362delinsTATTC
XM_011522192.1:c.*358_*362delinsTATTC	XP_011520494.1:n.*358_*362delinsTATTC
XM_005254987.3:c.*953_*957delinsTATTC	XP_005255044.1:n.*953_*957delinsTATTC
XM_006720759.2:c.*1004_*1008delinsTATTC	XP_006720822.1:n.*1004_*1008delinsTATTC
XM_006720760.2:c.*416_*420delinsTATTC	XP_006720823.1:n.*416_*420delinsTATTC
XM_011522187.2:c.*358_*362delinsTATTC	XP_011520489.1:n.*358_*362delinsTATTC
XM_011522188.3:c.*358_*362delinsTATTC	XP_011520490.1:n.*358_*362delinsTATTC
XM_011522189.2:c.*358_*362delinsTATTC	XP_011520491.1:n.*358_*362delinsTATTC
XM_011522191.3:c.*455_*459delinsTATTC	XP_011520493.1:n.*455_*459delinsTATTC
XM_011522192.2:c.*358_*362delinsTATTC	XP_011520494.1:n.*358_*362delinsTATTC
XM_017022712.2:c.*910_*914delinsTATTC	XP_016878201.1:n.*910_*914delinsTATTC
XM_017022713.2:c.*910_*914delinsTATTC	XP_016878202.1:n.*910_*914delinsTATTC
XM_017022715.2:c.*910_*914delinsTATTC	XP_016878204.1:n.*910_*914delinsTATTC
XM_017022716.2:c.*910_*914delinsTATTC	XP_016878205.1:n.*910_*914delinsTATTC
XM_017022717.1:c.*953_*957delinsTATTC	XP_016878206.1:n.*953_*957delinsTATTC
NM_003981.4:c.*910_*914delinsTATTC MANE Select	NP_003972.2:n.*910_*914delinsTATTC
NM_001267580.2:c.*953_*957delinsTATTC	NP_001254509.2:n.*953_*957delinsTATTC
NM_199413.3:c.*910_*914delinsTATTC	NP_955445.2:n.*910_*914delinsTATTC