Canonical Allele Identifier: CA1995653417

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050832_101050835delinsATTG , CM000673.2:g.101050832_101050835delinsATTG	GRCh38
NC_000011.9:g.100921563_100921566delinsATTG , CM000673.1:g.100921563_100921566delinsATTG	GRCh37
NC_000011.8:g.100426773_100426776delinsATTG	NCBI36
NG_016475.1:g.83979_83982delinsCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+589_2357+592delinsCAAT MANE Select	ENSP00000325120.5:n.2357+589_2357+592delinsCAAT
ENST00000263463.9:c.2051+589_2051+592delinsCAAT	ENSP00000263463.5:n.2051+589_2051+592delinsCAAT
ENST00000325455.9:c.2357+589_2357+592delinsCAAT	ENSP00000325120.5:n.2357+589_2357+592delinsCAAT
ENST00000526300.5:c.2051+589_2051+592delinsCAAT	ENSP00000436803.1:n.2051+589_2051+592delinsCAAT
ENST00000528960.5:c.2240+589_2240+592delinsCAAT	ENSP00000432914.1:n.2240+589_2240+592delinsCAAT
ENST00000530764.1:n.47+589_47+592delinsCAAT
ENST00000533207.5:n.1724+589_1724+592delinsCAAT
ENST00000534013.5:c.575+589_575+592delinsCAAT	ENSP00000436561.1:n.575+589_575+592delinsCAAT
ENST00000534780.5:c.2357+589_2357+592delinsCAAT	ENSP00000432352.1:n.2357+589_2357+592delinsCAAT
ENST00000617858.4:c.2052+114_2052+117delinsCAAT	ENSP00000481227.1:n.2052+114_2052+117delinsCAAT
ENST00000619228.2:c.2240+589_2240+592delinsCAAT	ENSP00000482698.1:n.2240+589_2240+592delinsCAAT
NM_000926.4:c.2357+589_2357+592delinsCAAT MANE Select	NP_000917.3:n.2357+589_2357+592delinsCAAT
NM_001202474.3:c.1865+589_1865+592delinsCAAT	NP_001189403.1:n.1865+589_1865+592delinsCAAT
NM_001271161.2:c.1559+589_1559+592delinsCAAT	NP_001258090.1:n.1559+589_1559+592delinsCAAT
NM_001271162.1:c.575+589_575+592delinsCAAT	NP_001258091.1:n.575+589_575+592delinsCAAT
NR_073141.2:n.2350+589_2350+592delinsCAAT
NR_073142.2:n.2233+589_2233+592delinsCAAT
NR_073143.2:n.2044+589_2044+592delinsCAAT
XM_006718858.2:c.2357+589_2357+592delinsCAAT	XP_006718921.1:n.2357+589_2357+592delinsCAAT
XM_006718858.3:c.2357+589_2357+592delinsCAAT	XP_006718921.1:n.2357+589_2357+592delinsCAAT
NM_001271162.2:c.575+589_575+592delinsCAAT	NP_001258091.1:n.575+589_575+592delinsCAAT
NR_073141.3:n.2364+589_2364+592delinsCAAT
NR_073142.3:n.2247+589_2247+592delinsCAAT
NR_073143.3:n.2058+589_2058+592delinsCAAT