Canonical Allele Identifier: CA7743777

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs137904575
• ExAC: 15:91509847 GACAC / G
• gnomAD v2: 15-91509847-GACAC-G
• gnomAD v3: 15-90966617-GACAC-G
• gnomAD v4: 15-90966617-GACAC-G
• MyVariant Identifiers: chr15:g.91509848_91509851del (hg19) ; chr15:g.90966618_90966621del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966621_90966624del , CM000677.2:g.90966621_90966624del	GRCh38
NC_000015.9:g.91509851_91509854del , CM000677.1:g.91509851_91509854del	GRCh37
NC_000015.8:g.89310855_89310858del	NCBI36
NG_050647.1:g.33031_33034del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*510_*513del (PRC1) MANE Select	ENSP00000377793.3:n.*510_*513del
ENST00000643536.1:c.*4135_*4138del	ENSP00000494429.1:n.*4135_*4138del
ENST00000361188.9:c.*510_*513del (PRC1)	ENSP00000354679.5:n.*510_*513del
ENST00000394249.7:c.*510_*513del (PRC1)	ENSP00000377793.3:n.*510_*513del
ENST00000555455.5:c.674_677del (PRC1)
ENST00000556972.6:c.157_160del (PRC1)	ENSP00000456737.1:n.157_160del
NM_001267580.1:c.*553_*556del (PRC1)	NP_001254509.1:n.*553_*556del
NM_003981.3:c.*510_*513del (PRC1)	NP_003972.1:n.*510_*513del
NM_199413.2:c.*510_*513del (PRC1)	NP_955445.1:n.*510_*513del
NR_051984.1:n.253_256del (PRC1-AS1)
XM_005254987.1:c.*553_*556del (PRC1)	XP_005255044.1:n.*553_*556del
XM_006720759.1:c.*604_*607del (PRC1)	XP_006720822.1:n.*604_*607del
XM_006720760.1:c.*16_*19del (PRC1)	XP_006720823.1:n.*16_*19del
XM_011522187.1:c.1824_1827del (PRC1)	XP_011520489.1:p.Cys609ArgfsTer3
XM_011522188.1:c.1782_1785del (PRC1)	XP_011520490.1:p.Cys595ArgfsTer3
XM_011522189.1:c.1713_1716del (PRC1)	XP_011520491.1:p.Cys572ArgfsTer3
XM_011522190.1:c.1653_1656del (PRC1)	XP_011520492.1:p.Cys552ArgfsTer3
XM_011522191.1:c.*55_*58del (PRC1)	XP_011520493.1:n.*55_*58del
XM_011522192.1:c.1503_1506del (PRC1)	XP_011520494.1:p.Cys502ArgfsTer3
XM_005254987.3:c.*553_*556del (PRC1)	XP_005255044.1:n.*553_*556del
XM_006720759.2:c.*604_*607del (PRC1)	XP_006720822.1:n.*604_*607del
XM_006720760.2:c.*16_*19del (PRC1)	XP_006720823.1:n.*16_*19del
XM_011522187.2:c.1824_1827del (PRC1)	XP_011520489.1:p.Cys609ArgfsTer3
XM_011522188.3:c.1782_1785del (PRC1)	XP_011520490.1:p.Cys595ArgfsTer3
XM_011522189.2:c.1713_1716del (PRC1)	XP_011520491.1:p.Cys572ArgfsTer3
XM_011522190.3:c.1653_1656del (PRC1)	XP_011520492.1:p.Cys552ArgfsTer3
XM_011522191.3:c.*55_*58del (PRC1)	XP_011520493.1:n.*55_*58del
XM_011522192.2:c.1503_1506del (PRC1)	XP_011520494.1:p.Cys502ArgfsTer3
XM_017022712.2:c.*510_*513del (PRC1)	XP_016878201.1:n.*510_*513del
XM_017022713.2:c.*510_*513del (PRC1)	XP_016878202.1:n.*510_*513del
XM_017022714.2:c.1668_1671del (PRC1)	XP_016878203.1:p.Cys557ArgfsTer3
XM_017022715.2:c.*510_*513del (PRC1)	XP_016878204.1:n.*510_*513del
XM_017022716.2:c.*510_*513del (PRC1)	XP_016878205.1:n.*510_*513del
XM_017022717.1:c.*553_*556del (PRC1)	XP_016878206.1:n.*553_*556del
NM_003981.4:c.*510_*513del (PRC1) MANE Select	NP_003972.2:n.*510_*513del
NM_001267580.2:c.*553_*556del (PRC1)	NP_001254509.2:n.*553_*556del
NM_199413.3:c.*510_*513del (PRC1)	NP_955445.2:n.*510_*513del