Canonical Allele Identifier: CA2195381205

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966365_90966369delinsGAACA , CM000677.2:g.90966365_90966369delinsGAACA	GRCh38
NC_000015.9:g.91509595_91509599delinsGAACA , CM000677.1:g.91509595_91509599delinsGAACA	GRCh37
NC_000015.8:g.89310599_89310603delinsGAACA	NCBI36
NG_050647.1:g.33283_33287delinsTGTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000394249.8:c.*762_*766delinsTGTTC MANE Select	ENSP00000377793.3:n.*762_*766delinsTGTTC
ENST00000643536.1:c.*4387_*4391delinsTGTTC	ENSP00000494429.1:n.*4387_*4391delinsTGTT...
ENST00000361188.9:c.*762_*766delinsTGTTC	ENSP00000354679.5:n.*762_*766delinsTGTTC
ENST00000394249.7:c.*762_*766delinsTGTTC	ENSP00000377793.3:n.*762_*766delinsTGTTC
ENST00000556972.6:c.409_413delinsTGTTC	ENSP00000456737.1:n.409_413delinsTGTTC
NM_001267580.1:c.*805_*809delinsTGTTC	NP_001254509.1:n.*805_*809delinsTGTTC
NM_003981.3:c.*762_*766delinsTGTTC	NP_003972.1:n.*762_*766delinsTGTTC
NM_199413.2:c.*762_*766delinsTGTTC	NP_955445.1:n.*762_*766delinsTGTTC
XM_005254987.1:c.*805_*809delinsTGTTC	XP_005255044.1:n.*805_*809delinsTGTTC
XM_006720759.1:c.*856_*860delinsTGTTC	XP_006720822.1:n.*856_*860delinsTGTTC
XM_006720760.1:c.*268_*272delinsTGTTC	XP_006720823.1:n.*268_*272delinsTGTTC
XM_011522187.1:c.*210_*214delinsTGTTC	XP_011520489.1:n.*210_*214delinsTGTTC
XM_011522188.1:c.*210_*214delinsTGTTC	XP_011520490.1:n.*210_*214delinsTGTTC
XM_011522189.1:c.*210_*214delinsTGTTC	XP_011520491.1:n.*210_*214delinsTGTTC
XM_011522190.1:c.*210_*214delinsTGTTC	XP_011520492.1:n.*210_*214delinsTGTTC
XM_011522192.1:c.*210_*214delinsTGTTC	XP_011520494.1:n.*210_*214delinsTGTTC
XM_005254987.3:c.*805_*809delinsTGTTC	XP_005255044.1:n.*805_*809delinsTGTTC
XM_006720759.2:c.*856_*860delinsTGTTC	XP_006720822.1:n.*856_*860delinsTGTTC
XM_006720760.2:c.*268_*272delinsTGTTC	XP_006720823.1:n.*268_*272delinsTGTTC
XM_011522187.2:c.*210_*214delinsTGTTC	XP_011520489.1:n.*210_*214delinsTGTTC
XM_011522188.3:c.*210_*214delinsTGTTC	XP_011520490.1:n.*210_*214delinsTGTTC
XM_011522189.2:c.*210_*214delinsTGTTC	XP_011520491.1:n.*210_*214delinsTGTTC
XM_011522191.3:c.*307_*311delinsTGTTC	XP_011520493.1:n.*307_*311delinsTGTTC
XM_011522192.2:c.*210_*214delinsTGTTC	XP_011520494.1:n.*210_*214delinsTGTTC
XM_017022712.2:c.*762_*766delinsTGTTC	XP_016878201.1:n.*762_*766delinsTGTTC
XM_017022713.2:c.*762_*766delinsTGTTC	XP_016878202.1:n.*762_*766delinsTGTTC
XM_017022715.2:c.*762_*766delinsTGTTC	XP_016878204.1:n.*762_*766delinsTGTTC
XM_017022716.2:c.*762_*766delinsTGTTC	XP_016878205.1:n.*762_*766delinsTGTTC
XM_017022717.1:c.*805_*809delinsTGTTC	XP_016878206.1:n.*805_*809delinsTGTTC
NM_003981.4:c.*762_*766delinsTGTTC MANE Select	NP_003972.2:n.*762_*766delinsTGTTC
NM_001267580.2:c.*805_*809delinsTGTTC	NP_001254509.2:n.*805_*809delinsTGTTC
NM_199413.3:c.*762_*766delinsTGTTC	NP_955445.2:n.*762_*766delinsTGTTC