Canonical Allele Identifier: CA717053157

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs1243642898
• gnomAD v3: 15-90966506-ACCC-A
• gnomAD v4: 15-90966506-ACCC-A
• MyVariant Identifiers: chr15:g.91509737_91509739del (hg19) ; chr15:g.90966507_90966509del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966509_90966511del , CM000677.2:g.90966509_90966511del	GRCh38
NC_000015.9:g.91509739_91509741del , CM000677.1:g.91509739_91509741del	GRCh37
NC_000015.8:g.89310743_89310745del	NCBI36
NG_050647.1:g.33143_33145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*622_*624del (PRC1) MANE Select	ENSP00000377793.3:n.*622_*624del
ENST00000643536.1:c.*4247_*4249del	ENSP00000494429.1:n.*4247_*4249del
ENST00000361188.9:c.*622_*624del (PRC1)	ENSP00000354679.5:n.*622_*624del
ENST00000394249.7:c.*622_*624del (PRC1)	ENSP00000377793.3:n.*622_*624del
ENST00000555455.5:c.786_788del (PRC1)
ENST00000556972.6:c.269_271del (PRC1)	ENSP00000456737.1:n.269_271del
NM_001267580.1:c.*665_*667del (PRC1)	NP_001254509.1:n.*665_*667del
NM_003981.3:c.*622_*624del (PRC1)	NP_003972.1:n.*622_*624del
NM_199413.2:c.*622_*624del (PRC1)	NP_955445.1:n.*622_*624del
NR_051984.1:n.141_143del (PRC1-AS1)
XM_005254987.1:c.*665_*667del (PRC1)	XP_005255044.1:n.*665_*667del
XM_006720759.1:c.*716_*718del (PRC1)	XP_006720822.1:n.*716_*718del
XM_006720760.1:c.*128_*130del (PRC1)	XP_006720823.1:n.*128_*130del
XM_011522187.1:c.*70_*72del (PRC1)	XP_011520489.1:n.*70_*72del
XM_011522188.1:c.*70_*72del (PRC1)	XP_011520490.1:n.*70_*72del
XM_011522189.1:c.*70_*72del (PRC1)	XP_011520491.1:n.*70_*72del
XM_011522190.1:c.*70_*72del (PRC1)	XP_011520492.1:n.*70_*72del
XM_011522192.1:c.*70_*72del (PRC1)	XP_011520494.1:n.*70_*72del
XM_005254987.3:c.*665_*667del (PRC1)	XP_005255044.1:n.*665_*667del
XM_006720759.2:c.*716_*718del (PRC1)	XP_006720822.1:n.*716_*718del
XM_006720760.2:c.*128_*130del (PRC1)	XP_006720823.1:n.*128_*130del
XM_011522187.2:c.*70_*72del (PRC1)	XP_011520489.1:n.*70_*72del
XM_011522188.3:c.*70_*72del (PRC1)	XP_011520490.1:n.*70_*72del
XM_011522189.2:c.*70_*72del (PRC1)	XP_011520491.1:n.*70_*72del
XM_011522191.3:c.*167_*169del (PRC1)	XP_011520493.1:n.*167_*169del
XM_011522192.2:c.*70_*72del (PRC1)	XP_011520494.1:n.*70_*72del
XM_017022712.2:c.*622_*624del (PRC1)	XP_016878201.1:n.*622_*624del
XM_017022713.2:c.*622_*624del (PRC1)	XP_016878202.1:n.*622_*624del
XM_017022715.2:c.*622_*624del (PRC1)	XP_016878204.1:n.*622_*624del
XM_017022716.2:c.*622_*624del (PRC1)	XP_016878205.1:n.*622_*624del
XM_017022717.1:c.*665_*667del (PRC1)	XP_016878206.1:n.*665_*667del
NM_003981.4:c.*622_*624del (PRC1) MANE Select	NP_003972.2:n.*622_*624del
NM_001267580.2:c.*665_*667del (PRC1)	NP_001254509.2:n.*665_*667del
NM_199413.3:c.*622_*624del (PRC1)	NP_955445.2:n.*622_*624del