Canonical Allele Identifier: CA1995654102

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051233_101051234delinsAG , CM000673.2:g.101051233_101051234delinsAG	GRCh38
NC_000011.9:g.100921964_100921965delinsAG , CM000673.1:g.100921964_100921965delinsAG	GRCh37
NC_000011.8:g.100427174_100427175delinsAG	NCBI36
NG_016475.1:g.83580_83581delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+190_2357+191delinsCT MANE Select	ENSP00000325120.5:n.2357+190_2357+191delinsCT
ENST00000263463.9:c.2051+190_2051+191delinsCT	ENSP00000263463.5:n.2051+190_2051+191delinsCT
ENST00000325455.9:c.2357+190_2357+191delinsCT	ENSP00000325120.5:n.2357+190_2357+191delinsCT
ENST00000526300.5:c.2051+190_2051+191delinsCT	ENSP00000436803.1:n.2051+190_2051+191delinsCT
ENST00000528960.5:c.2240+190_2240+191delinsCT	ENSP00000432914.1:n.2240+190_2240+191delinsCT
ENST00000530764.1:n.47+190_47+191delinsCT
ENST00000533207.5:n.1724+190_1724+191delinsCT
ENST00000534013.5:c.575+190_575+191delinsCT	ENSP00000436561.1:n.575+190_575+191delinsCT
ENST00000534780.5:c.2357+190_2357+191delinsCT	ENSP00000432352.1:n.2357+190_2357+191delinsCT
ENST00000617858.4:c.2051+190_2051+191delinsCT	ENSP00000481227.1:n.2051+190_2051+191delinsCT
ENST00000619228.2:c.2240+190_2240+191delinsCT	ENSP00000482698.1:n.2240+190_2240+191delinsCT
NM_000926.4:c.2357+190_2357+191delinsCT MANE Select	NP_000917.3:n.2357+190_2357+191delinsCT
NM_001202474.3:c.1865+190_1865+191delinsCT	NP_001189403.1:n.1865+190_1865+191delinsCT
NM_001271161.2:c.1559+190_1559+191delinsCT	NP_001258090.1:n.1559+190_1559+191delinsCT
NM_001271162.1:c.575+190_575+191delinsCT	NP_001258091.1:n.575+190_575+191delinsCT
NR_073141.2:n.2350+190_2350+191delinsCT
NR_073142.2:n.2233+190_2233+191delinsCT
NR_073143.2:n.2044+190_2044+191delinsCT
XM_006718858.2:c.2357+190_2357+191delinsCT	XP_006718921.1:n.2357+190_2357+191delinsCT
XM_006718858.3:c.2357+190_2357+191delinsCT	XP_006718921.1:n.2357+190_2357+191delinsCT
NM_001271162.2:c.575+190_575+191delinsCT	NP_001258091.1:n.575+190_575+191delinsCT
NR_073141.3:n.2364+190_2364+191delinsCT
NR_073142.3:n.2247+190_2247+191delinsCT
NR_073143.3:n.2058+190_2058+191delinsCT