Canonical Allele Identifier: CA601426508
Gene: PGR HGNC NCBI

Linked Data

dbSNP Id: rs1181367181

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051053_101051056del , CM000673.2:g.101051053_101051056del GRCh38
NC_000011.9:g.100921784_100921787del , CM000673.1:g.100921784_100921787del GRCh37
NC_000011.8:g.100426994_100426997del NCBI36
NG_016475.1:g.83759_83762del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2357+369_2357+372del MANE Select ENSP00000325120.5:n.2357+369_2357+372del
ENST00000263463.9:c.2051+369_2051+372del ENSP00000263463.5:n.2051+369_2051+372del
ENST00000325455.9:c.2357+369_2357+372del ENSP00000325120.5:n.2357+369_2357+372del
ENST00000526300.5:c.2051+369_2051+372del ENSP00000436803.1:n.2051+369_2051+372del
ENST00000528960.5:c.2240+369_2240+372del ENSP00000432914.1:n.2240+369_2240+372del
ENST00000530764.1:n.47+369_47+372del
ENST00000533207.5:n.1724+369_1724+372del
ENST00000534013.5:c.575+369_575+372del ENSP00000436561.1:n.575+369_575+372del
ENST00000534780.5:c.2357+369_2357+372del ENSP00000432352.1:n.2357+369_2357+372del
ENST00000617858.4:c.2052-106_2052-103del ENSP00000481227.1:n.2052-106_2052-103del
ENST00000619228.2:c.2240+369_2240+372del ENSP00000482698.1:n.2240+369_2240+372del
NM_000926.4:c.2357+369_2357+372del MANE Select NP_000917.3:n.2357+369_2357+372del
NM_001202474.3:c.1865+369_1865+372del NP_001189403.1:n.1865+369_1865+372del
NM_001271161.2:c.1559+369_1559+372del NP_001258090.1:n.1559+369_1559+372del
NM_001271162.1:c.575+369_575+372del NP_001258091.1:n.575+369_575+372del
NR_073141.2:n.2350+369_2350+372del
NR_073142.2:n.2233+369_2233+372del
NR_073143.2:n.2044+369_2044+372del
XM_006718858.2:c.2357+369_2357+372del XP_006718921.1:n.2357+369_2357+372del
XM_006718858.3:c.2357+369_2357+372del XP_006718921.1:n.2357+369_2357+372del
NM_001271162.2:c.575+369_575+372del NP_001258091.1:n.575+369_575+372del
NR_073141.3:n.2364+369_2364+372del
NR_073142.3:n.2247+369_2247+372del
NR_073143.3:n.2058+369_2058+372del