Canonical Allele Identifier: CA1995654200

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051278_101051279delinsAG , CM000673.2:g.101051278_101051279delinsAG	GRCh38
NC_000011.9:g.100922009_100922010delinsAG , CM000673.1:g.100922009_100922010delinsAG	GRCh37
NC_000011.8:g.100427219_100427220delinsAG	NCBI36
NG_016475.1:g.83535_83536delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+145_2357+146delinsCT MANE Select	ENSP00000325120.5:n.2357+145_2357+146delinsCT
ENST00000263463.9:c.2051+145_2051+146delinsCT	ENSP00000263463.5:n.2051+145_2051+146delinsCT
ENST00000325455.9:c.2357+145_2357+146delinsCT	ENSP00000325120.5:n.2357+145_2357+146delinsCT
ENST00000526300.5:c.2051+145_2051+146delinsCT	ENSP00000436803.1:n.2051+145_2051+146delinsCT
ENST00000528960.5:c.2240+145_2240+146delinsCT	ENSP00000432914.1:n.2240+145_2240+146delinsCT
ENST00000530764.1:n.47+145_47+146delinsCT
ENST00000533207.5:n.1724+145_1724+146delinsCT
ENST00000534013.5:c.575+145_575+146delinsCT	ENSP00000436561.1:n.575+145_575+146delinsCT
ENST00000534780.5:c.2357+145_2357+146delinsCT	ENSP00000432352.1:n.2357+145_2357+146delinsCT
ENST00000617858.4:c.2051+145_2051+146delinsCT	ENSP00000481227.1:n.2051+145_2051+146delinsCT
ENST00000619228.2:c.2240+145_2240+146delinsCT	ENSP00000482698.1:n.2240+145_2240+146delinsCT
NM_000926.4:c.2357+145_2357+146delinsCT MANE Select	NP_000917.3:n.2357+145_2357+146delinsCT
NM_001202474.3:c.1865+145_1865+146delinsCT	NP_001189403.1:n.1865+145_1865+146delinsCT
NM_001271161.2:c.1559+145_1559+146delinsCT	NP_001258090.1:n.1559+145_1559+146delinsCT
NM_001271162.1:c.575+145_575+146delinsCT	NP_001258091.1:n.575+145_575+146delinsCT
NR_073141.2:n.2350+145_2350+146delinsCT
NR_073142.2:n.2233+145_2233+146delinsCT
NR_073143.2:n.2044+145_2044+146delinsCT
XM_006718858.2:c.2357+145_2357+146delinsCT	XP_006718921.1:n.2357+145_2357+146delinsCT
XM_006718858.3:c.2357+145_2357+146delinsCT	XP_006718921.1:n.2357+145_2357+146delinsCT
NM_001271162.2:c.575+145_575+146delinsCT	NP_001258091.1:n.575+145_575+146delinsCT
NR_073141.3:n.2364+145_2364+146delinsCT
NR_073142.3:n.2247+145_2247+146delinsCT
NR_073143.3:n.2058+145_2058+146delinsCT