Canonical Allele Identifier: CA1995653863

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051078_101051082delinsGAAGA , CM000673.2:g.101051078_101051082delinsGAAGA	GRCh38
NC_000011.9:g.100921809_100921813delinsGAAGA , CM000673.1:g.100921809_100921813delinsGAAGA	GRCh37
NC_000011.8:g.100427019_100427023delinsGAAGA	NCBI36
NG_016475.1:g.83732_83736delinsTCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+342_2357+346delinsTCTTC MANE Select	ENSP00000325120.5:n.2357+342_2357+346delinsTCTTC
ENST00000263463.9:c.2051+342_2051+346delinsTCTTC	ENSP00000263463.5:n.2051+342_2051+346delinsTCTTC
ENST00000325455.9:c.2357+342_2357+346delinsTCTTC	ENSP00000325120.5:n.2357+342_2357+346delinsTCTTC
ENST00000526300.5:c.2051+342_2051+346delinsTCTTC	ENSP00000436803.1:n.2051+342_2051+346delinsTCTTC
ENST00000528960.5:c.2240+342_2240+346delinsTCTTC	ENSP00000432914.1:n.2240+342_2240+346delinsTCTTC
ENST00000530764.1:n.47+342_47+346delinsTCTTC
ENST00000533207.5:n.1724+342_1724+346delinsTCTTC
ENST00000534013.5:c.575+342_575+346delinsTCTTC	ENSP00000436561.1:n.575+342_575+346delinsTCTTC
ENST00000534780.5:c.2357+342_2357+346delinsTCTTC	ENSP00000432352.1:n.2357+342_2357+346delinsTCTTC
ENST00000617858.4:c.2052-133_2052-129delinsTCTTC	ENSP00000481227.1:n.2052-133_2052-129delinsTCTTC
ENST00000619228.2:c.2240+342_2240+346delinsTCTTC	ENSP00000482698.1:n.2240+342_2240+346delinsTCTTC
NM_000926.4:c.2357+342_2357+346delinsTCTTC MANE Select	NP_000917.3:n.2357+342_2357+346delinsTCTTC
NM_001202474.3:c.1865+342_1865+346delinsTCTTC	NP_001189403.1:n.1865+342_1865+346delinsTCTTC
NM_001271161.2:c.1559+342_1559+346delinsTCTTC	NP_001258090.1:n.1559+342_1559+346delinsTCTTC
NM_001271162.1:c.575+342_575+346delinsTCTTC	NP_001258091.1:n.575+342_575+346delinsTCTTC
NR_073141.2:n.2350+342_2350+346delinsTCTTC
NR_073142.2:n.2233+342_2233+346delinsTCTTC
NR_073143.2:n.2044+342_2044+346delinsTCTTC
XM_006718858.2:c.2357+342_2357+346delinsTCTTC	XP_006718921.1:n.2357+342_2357+346delinsTCTTC
XM_006718858.3:c.2357+342_2357+346delinsTCTTC	XP_006718921.1:n.2357+342_2357+346delinsTCTTC
NM_001271162.2:c.575+342_575+346delinsTCTTC	NP_001258091.1:n.575+342_575+346delinsTCTTC
NR_073141.3:n.2364+342_2364+346delinsTCTTC
NR_073142.3:n.2247+342_2247+346delinsTCTTC
NR_073143.3:n.2058+342_2058+346delinsTCTTC