Canonical Allele Identifier: CA2510590458

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050925_101051007del , CM000673.2:g.101050925_101051007del	GRCh38
NC_000011.9:g.100921656_100921738del , CM000673.1:g.100921656_100921738del	GRCh37
NC_000011.8:g.100426866_100426948del	NCBI36
NG_016475.1:g.83812_83894del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+422_2357+504del MANE Select	ENSP00000325120.5:n.2357+422_2357+504del
ENST00000263463.9:c.2051+422_2051+504del	ENSP00000263463.5:n.2051+422_2051+504del
ENST00000325455.9:c.2357+422_2357+504del	ENSP00000325120.5:n.2357+422_2357+504del
ENST00000526300.5:c.2051+422_2051+504del	ENSP00000436803.1:n.2051+422_2051+504del
ENST00000528960.5:c.2240+422_2240+504del	ENSP00000432914.1:n.2240+422_2240+504del
ENST00000530764.1:n.47+422_47+504del
ENST00000533207.5:n.1724+422_1724+504del
ENST00000534013.5:c.575+422_575+504del	ENSP00000436561.1:n.575+422_575+504del
ENST00000534780.5:c.2357+422_2357+504del	ENSP00000432352.1:n.2357+422_2357+504del
ENST00000617858.4:c.2052-53_2052+29del
ENST00000619228.2:c.2240+422_2240+504del	ENSP00000482698.1:n.2240+422_2240+504del
NM_000926.4:c.2357+422_2357+504del MANE Select	NP_000917.3:n.2357+422_2357+504del
NM_001202474.3:c.1865+422_1865+504del	NP_001189403.1:n.1865+422_1865+504del
NM_001271161.2:c.1559+422_1559+504del	NP_001258090.1:n.1559+422_1559+504del
NM_001271162.1:c.575+422_575+504del	NP_001258091.1:n.575+422_575+504del
NR_073141.2:n.2350+422_2350+504del
NR_073142.2:n.2233+422_2233+504del
NR_073143.2:n.2044+422_2044+504del
XM_006718858.2:c.2357+422_2357+504del	XP_006718921.1:n.2357+422_2357+504del
XM_006718858.3:c.2357+422_2357+504del	XP_006718921.1:n.2357+422_2357+504del
NM_001271162.2:c.575+422_575+504del	NP_001258091.1:n.575+422_575+504del
NR_073141.3:n.2364+422_2364+504del
NR_073142.3:n.2247+422_2247+504del
NR_073143.3:n.2058+422_2058+504del