Canonical Allele Identifier: CA2195380870

Gene: PRC1

Linked Data

• dbSNP Id: rs2037465877

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966113_90966123del , CM000677.2:g.90966113_90966123del	GRCh38
NC_000015.9:g.91509343_91509353del , CM000677.1:g.91509343_91509353del	GRCh37
NC_000015.8:g.89310347_89310357del	NCBI36
NG_050647.1:g.33532_33542del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*1011_*1021del MANE Select	ENSP00000377793.3:n.*1011_*1021del
ENST00000361188.9:c.*1011_*1021del	ENSP00000354679.5:n.*1011_*1021del
ENST00000394249.7:c.*1011_*1021del	ENSP00000377793.3:n.*1011_*1021del
ENST00000556972.6:c.658_668del	ENSP00000456737.1:n.658_668del
NM_001267580.1:c.*1054_*1064del	NP_001254509.1:n.*1054_*1064del
NM_003981.3:c.*1011_*1021del	NP_003972.1:n.*1011_*1021del
NM_199413.2:c.*1011_*1021del	NP_955445.1:n.*1011_*1021del
XM_005254987.1:c.*1054_*1064del	XP_005255044.1:n.*1054_*1064del
XM_006720759.1:c.*1105_*1115del	XP_006720822.1:n.*1105_*1115del
XM_006720760.1:c.*517_*527del	XP_006720823.1:n.*517_*527del
XM_011522187.1:c.*459_*469del	XP_011520489.1:n.*459_*469del
XM_011522188.1:c.*459_*469del	XP_011520490.1:n.*459_*469del
XM_011522189.1:c.*459_*469del	XP_011520491.1:n.*459_*469del
XM_011522190.1:c.*459_*469del	XP_011520492.1:n.*459_*469del
XM_011522192.1:c.*459_*469del	XP_011520494.1:n.*459_*469del
XM_005254987.3:c.*1054_*1064del	XP_005255044.1:n.*1054_*1064del
XM_006720759.2:c.*1105_*1115del	XP_006720822.1:n.*1105_*1115del
XM_006720760.2:c.*517_*527del	XP_006720823.1:n.*517_*527del
XM_011522187.2:c.*459_*469del	XP_011520489.1:n.*459_*469del
XM_011522188.3:c.*459_*469del	XP_011520490.1:n.*459_*469del
XM_011522189.2:c.*459_*469del	XP_011520491.1:n.*459_*469del
XM_011522191.3:c.*556_*566del	XP_011520493.1:n.*556_*566del
XM_011522192.2:c.*459_*469del	XP_011520494.1:n.*459_*469del
XM_017022712.2:c.*1011_*1021del	XP_016878201.1:n.*1011_*1021del
XM_017022713.2:c.*1011_*1021del	XP_016878202.1:n.*1011_*1021del
XM_017022715.2:c.*1011_*1021del	XP_016878204.1:n.*1011_*1021del
XM_017022716.2:c.*1011_*1021del	XP_016878205.1:n.*1011_*1021del
XM_017022717.1:c.*1054_*1064del	XP_016878206.1:n.*1054_*1064del
NM_003981.4:c.*1011_*1021del MANE Select	NP_003972.2:n.*1011_*1021del
NM_001267580.2:c.*1054_*1064del	NP_001254509.2:n.*1054_*1064del
NM_199413.3:c.*1011_*1021del	NP_955445.2:n.*1011_*1021del