Canonical Allele Identifier: CA2195381042

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966235_90966238delinsCAAG , CM000677.2:g.90966235_90966238delinsCAAG	GRCh38
NC_000015.9:g.91509465_91509468delinsCAAG , CM000677.1:g.91509465_91509468delinsCAAG	GRCh37
NC_000015.8:g.89310469_89310472delinsCAAG	NCBI36
NG_050647.1:g.33414_33417delinsCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*893_*896delinsCTTG MANE Select	ENSP00000377793.3:n.*893_*896delinsCTTG
ENST00000643536.1:c.*4518_*4521delinsCTTG	ENSP00000494429.1:n.*4518_*4521delinsCTTG
ENST00000361188.9:c.*893_*896delinsCTTG	ENSP00000354679.5:n.*893_*896delinsCTTG
ENST00000394249.7:c.*893_*896delinsCTTG	ENSP00000377793.3:n.*893_*896delinsCTTG
ENST00000556972.6:c.540_543delinsCTTG	ENSP00000456737.1:n.540_543delinsCTTG
NM_001267580.1:c.*936_*939delinsCTTG	NP_001254509.1:n.*936_*939delinsCTTG
NM_003981.3:c.*893_*896delinsCTTG	NP_003972.1:n.*893_*896delinsCTTG
NM_199413.2:c.*893_*896delinsCTTG	NP_955445.1:n.*893_*896delinsCTTG
XM_005254987.1:c.*936_*939delinsCTTG	XP_005255044.1:n.*936_*939delinsCTTG
XM_006720759.1:c.*987_*990delinsCTTG	XP_006720822.1:n.*987_*990delinsCTTG
XM_006720760.1:c.*399_*402delinsCTTG	XP_006720823.1:n.*399_*402delinsCTTG
XM_011522187.1:c.*341_*344delinsCTTG	XP_011520489.1:n.*341_*344delinsCTTG
XM_011522188.1:c.*341_*344delinsCTTG	XP_011520490.1:n.*341_*344delinsCTTG
XM_011522189.1:c.*341_*344delinsCTTG	XP_011520491.1:n.*341_*344delinsCTTG
XM_011522190.1:c.*341_*344delinsCTTG	XP_011520492.1:n.*341_*344delinsCTTG
XM_011522192.1:c.*341_*344delinsCTTG	XP_011520494.1:n.*341_*344delinsCTTG
XM_005254987.3:c.*936_*939delinsCTTG	XP_005255044.1:n.*936_*939delinsCTTG
XM_006720759.2:c.*987_*990delinsCTTG	XP_006720822.1:n.*987_*990delinsCTTG
XM_006720760.2:c.*399_*402delinsCTTG	XP_006720823.1:n.*399_*402delinsCTTG
XM_011522187.2:c.*341_*344delinsCTTG	XP_011520489.1:n.*341_*344delinsCTTG
XM_011522188.3:c.*341_*344delinsCTTG	XP_011520490.1:n.*341_*344delinsCTTG
XM_011522189.2:c.*341_*344delinsCTTG	XP_011520491.1:n.*341_*344delinsCTTG
XM_011522191.3:c.*438_*441delinsCTTG	XP_011520493.1:n.*438_*441delinsCTTG
XM_011522192.2:c.*341_*344delinsCTTG	XP_011520494.1:n.*341_*344delinsCTTG
XM_017022712.2:c.*893_*896delinsCTTG	XP_016878201.1:n.*893_*896delinsCTTG
XM_017022713.2:c.*893_*896delinsCTTG	XP_016878202.1:n.*893_*896delinsCTTG
XM_017022715.2:c.*893_*896delinsCTTG	XP_016878204.1:n.*893_*896delinsCTTG
XM_017022716.2:c.*893_*896delinsCTTG	XP_016878205.1:n.*893_*896delinsCTTG
XM_017022717.1:c.*936_*939delinsCTTG	XP_016878206.1:n.*936_*939delinsCTTG
NM_003981.4:c.*893_*896delinsCTTG MANE Select	NP_003972.2:n.*893_*896delinsCTTG
NM_001267580.2:c.*936_*939delinsCTTG	NP_001254509.2:n.*936_*939delinsCTTG
NM_199413.3:c.*893_*896delinsCTTG	NP_955445.2:n.*893_*896delinsCTTG