Canonical Allele Identifier: CA601426493
Gene: PGR HGNC NCBI

Linked Data

dbSNP Id: rs1415034070

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101050836_101050838del , CM000673.2:g.101050836_101050838del GRCh38
NC_000011.9:g.100921567_100921569del , CM000673.1:g.100921567_100921569del GRCh37
NC_000011.8:g.100426777_100426779del NCBI36
NG_016475.1:g.83979_83981del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2357+589_2357+591del MANE Select ENSP00000325120.5:n.2357+589_2357+591del
ENST00000263463.9:c.2051+589_2051+591del ENSP00000263463.5:n.2051+589_2051+591del
ENST00000325455.9:c.2357+589_2357+591del ENSP00000325120.5:n.2357+589_2357+591del
ENST00000526300.5:c.2051+589_2051+591del ENSP00000436803.1:n.2051+589_2051+591del
ENST00000528960.5:c.2240+589_2240+591del ENSP00000432914.1:n.2240+589_2240+591del
ENST00000530764.1:n.47+589_47+591del
ENST00000533207.5:n.1724+589_1724+591del
ENST00000534013.5:c.575+589_575+591del ENSP00000436561.1:n.575+589_575+591del
ENST00000534780.5:c.2357+589_2357+591del ENSP00000432352.1:n.2357+589_2357+591del
ENST00000617858.4:c.2052+114_2052+116del ENSP00000481227.1:n.2052+114_2052+116del
ENST00000619228.2:c.2240+589_2240+591del ENSP00000482698.1:n.2240+589_2240+591del
NM_000926.4:c.2357+589_2357+591del MANE Select NP_000917.3:n.2357+589_2357+591del
NM_001202474.3:c.1865+589_1865+591del NP_001189403.1:n.1865+589_1865+591del
NM_001271161.2:c.1559+589_1559+591del NP_001258090.1:n.1559+589_1559+591del
NM_001271162.1:c.575+589_575+591del NP_001258091.1:n.575+589_575+591del
NR_073141.2:n.2350+589_2350+591del
NR_073142.2:n.2233+589_2233+591del
NR_073143.2:n.2044+589_2044+591del
XM_006718858.2:c.2357+589_2357+591del XP_006718921.1:n.2357+589_2357+591del
XM_006718858.3:c.2357+589_2357+591del XP_006718921.1:n.2357+589_2357+591del
NM_001271162.2:c.575+589_575+591del NP_001258091.1:n.575+589_575+591del
NR_073141.3:n.2364+589_2364+591del
NR_073142.3:n.2247+589_2247+591del
NR_073143.3:n.2058+589_2058+591del