Canonical Allele Identifier: CA941519358

Gene: PGR

Linked Data

• dbSNP Id: rs1860071058

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051058_101051060del , CM000673.2:g.101051058_101051060del	GRCh38
NC_000011.9:g.100921789_100921791del , CM000673.1:g.100921789_100921791del	GRCh37
NC_000011.8:g.100426999_100427001del	NCBI36
NG_016475.1:g.83756_83758del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+366_2357+368del MANE Select	ENSP00000325120.5:n.2357+366_2357+368del
ENST00000263463.9:c.2051+366_2051+368del	ENSP00000263463.5:n.2051+366_2051+368del
ENST00000325455.9:c.2357+366_2357+368del	ENSP00000325120.5:n.2357+366_2357+368del
ENST00000526300.5:c.2051+366_2051+368del	ENSP00000436803.1:n.2051+366_2051+368del
ENST00000528960.5:c.2240+366_2240+368del	ENSP00000432914.1:n.2240+366_2240+368del
ENST00000530764.1:n.47+366_47+368del
ENST00000533207.5:n.1724+366_1724+368del
ENST00000534013.5:c.575+366_575+368del	ENSP00000436561.1:n.575+366_575+368del
ENST00000534780.5:c.2357+366_2357+368del	ENSP00000432352.1:n.2357+366_2357+368del
ENST00000617858.4:c.2052-109_2052-107del	ENSP00000481227.1:n.2052-109_2052-107del
ENST00000619228.2:c.2240+366_2240+368del	ENSP00000482698.1:n.2240+366_2240+368del
NM_000926.4:c.2357+366_2357+368del MANE Select	NP_000917.3:n.2357+366_2357+368del
NM_001202474.3:c.1865+366_1865+368del	NP_001189403.1:n.1865+366_1865+368del
NM_001271161.2:c.1559+366_1559+368del	NP_001258090.1:n.1559+366_1559+368del
NM_001271162.1:c.575+366_575+368del	NP_001258091.1:n.575+366_575+368del
NR_073141.2:n.2350+366_2350+368del
NR_073142.2:n.2233+366_2233+368del
NR_073143.2:n.2044+366_2044+368del
XM_006718858.2:c.2357+366_2357+368del	XP_006718921.1:n.2357+366_2357+368del
XM_006718858.3:c.2357+366_2357+368del	XP_006718921.1:n.2357+366_2357+368del
NM_001271162.2:c.575+366_575+368del	NP_001258091.1:n.575+366_575+368del
NR_073141.3:n.2364+366_2364+368del
NR_073142.3:n.2247+366_2247+368del
NR_073143.3:n.2058+366_2058+368del