Canonical Allele Identifier: CA2615679908
Gene: PGR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051500del , CM000673.2:g.101051500del GRCh38
NC_000011.9:g.100922231del , CM000673.1:g.100922231del GRCh37
NC_000011.8:g.100427441del NCBI36
NG_016475.1:g.83316del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2283del MANE Select ENSP00000325120.5:p.Phe761LeufsTer3
ENST00000263463.9:c.1977del ENSP00000263463.5:p.Phe659LeufsTer3
ENST00000325455.9:c.2283del ENSP00000325120.5:p.Phe761LeufsTer3
ENST00000526300.5:c.1977del ENSP00000436803.1:p.Phe659LeufsTer3
ENST00000528960.5:c.2166del ENSP00000432914.1:p.Phe722LeufsTer3
ENST00000533207.5:n.1650del
ENST00000534013.5:c.501del ENSP00000436561.1:p.Phe167LeufsTer3
ENST00000534780.5:c.2283del ENSP00000432352.1:p.Phe761LeufsTer3
ENST00000617858.4:c.1977del ENSP00000481227.1:p.Phe659LeufsTer3
ENST00000619228.2:c.2166del ENSP00000482698.1:p.Phe722LeufsTer3
NM_000926.4:c.2283del MANE Select NP_000917.3:p.Phe761LeufsTer3
NM_001202474.3:c.1791del NP_001189403.1:p.Phe597LeufsTer3
NM_001271161.2:c.1485del NP_001258090.1:p.Phe495LeufsTer3
NM_001271162.1:c.501del NP_001258091.1:p.Phe167LeufsTer3
NR_073141.2:n.2276del
NR_073142.2:n.2159del
NR_073143.2:n.1970del
XM_006718858.2:c.2283del XP_006718921.1:p.Phe761LeufsTer3
XR_947831.1:n.3964del
XM_006718858.3:c.2283del XP_006718921.1:p.Phe761LeufsTer3
NM_001271162.2:c.501del NP_001258091.1:p.Phe167LeufsTer3
NR_073141.3:n.2290del
NR_073142.3:n.2173del
NR_073143.3:n.1984del