Canonical Allele Identifier: CA2630415392

Gene: PRC1 PRC1-AS1

Linked Data

• gnomAD v4: 15-90966718-ATGCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966719_90966723del , CM000677.2:g.90966719_90966723del	GRCh38
NC_000015.9:g.91509949_91509953del , CM000677.1:g.91509949_91509953del	GRCh37
NC_000015.8:g.89310953_89310957del	NCBI36
NG_050647.1:g.32929_32933del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*408_*412del (PRC1) MANE Select	ENSP00000377793.3:n.*408_*412del
ENST00000643536.1:c.*4033_*4037del	ENSP00000494429.1:n.*4033_*4037del
ENST00000361188.9:c.*408_*412del (PRC1)	ENSP00000354679.5:n.*408_*412del
ENST00000394249.7:c.*408_*412del (PRC1)	ENSP00000377793.3:n.*408_*412del
ENST00000555455.5:c.642-70_642-66del (PRC1)
ENST00000556972.6:c.125-70_125-66del (PRC1)	ENSP00000456737.1:n.125-70_125-66del
ENST00000560423.5:c.696_700del (PRC1)
NM_001267580.1:c.*451_*455del (PRC1)	NP_001254509.1:n.*451_*455del
NM_003981.3:c.*408_*412del (PRC1)	NP_003972.1:n.*408_*412del
NM_199413.2:c.*408_*412del (PRC1)	NP_955445.1:n.*408_*412del
NR_051984.1:n.310+41_310+45del (PRC1-AS1)
XM_005254987.1:c.*451_*455del (PRC1)	XP_005255044.1:n.*451_*455del
XM_006720759.1:c.*502_*506del (PRC1)	XP_006720822.1:n.*502_*506del
XM_006720760.1:c.1673-70_1673-66del (PRC1)	XP_006720823.1:n.1673-70_1673-66del
XM_011522187.1:c.1792-70_1792-66del (PRC1)	XP_011520489.1:n.1792-70_1792-66del
XM_011522188.1:c.1750-70_1750-66del (PRC1)	XP_011520490.1:n.1750-70_1750-66del
XM_011522189.1:c.1681-70_1681-66del (PRC1)	XP_011520491.1:n.1681-70_1681-66del
XM_011522190.1:c.1621-70_1621-66del (PRC1)	XP_011520492.1:n.1621-70_1621-66del
XM_011522191.1:c.*23-70_*23-66del (PRC1)	XP_011520493.1:n.*23-70_*23-66del
XM_011522192.1:c.1471-70_1471-66del (PRC1)	XP_011520494.1:n.1471-70_1471-66del
XM_005254987.3:c.*451_*455del (PRC1)	XP_005255044.1:n.*451_*455del
XM_006720759.2:c.*502_*506del (PRC1)	XP_006720822.1:n.*502_*506del
XM_006720760.2:c.1673-70_1673-66del (PRC1)	XP_006720823.1:n.1673-70_1673-66del
XM_011522187.2:c.1792-70_1792-66del (PRC1)	XP_011520489.1:n.1792-70_1792-66del
XM_011522188.3:c.1750-70_1750-66del (PRC1)	XP_011520490.1:n.1750-70_1750-66del
XM_011522189.2:c.1681-70_1681-66del (PRC1)	XP_011520491.1:n.1681-70_1681-66del
XM_011522190.3:c.1621-70_1621-66del (PRC1)	XP_011520492.1:n.1621-70_1621-66del
XM_011522191.3:c.*23-70_*23-66del (PRC1)	XP_011520493.1:n.*23-70_*23-66del
XM_011522192.2:c.1471-70_1471-66del (PRC1)	XP_011520494.1:n.1471-70_1471-66del
XM_017022712.2:c.*408_*412del (PRC1)	XP_016878201.1:n.*408_*412del
XM_017022713.2:c.*408_*412del (PRC1)	XP_016878202.1:n.*408_*412del
XM_017022714.2:c.1636-70_1636-66del (PRC1)	XP_016878203.1:n.1636-70_1636-66del
XM_017022715.2:c.*408_*412del (PRC1)	XP_016878204.1:n.*408_*412del
XM_017022716.2:c.*408_*412del (PRC1)	XP_016878205.1:n.*408_*412del
XM_017022717.1:c.*451_*455del (PRC1)	XP_016878206.1:n.*451_*455del
NM_003981.4:c.*408_*412del (PRC1) MANE Select	NP_003972.2:n.*408_*412del
NM_001267580.2:c.*451_*455del (PRC1)	NP_001254509.2:n.*451_*455del
NM_199413.3:c.*408_*412del (PRC1)	NP_955445.2:n.*408_*412del