Canonical Allele Identifier: CA2505085173

Gene: PGR

Linked Data

• gnomAD v4: 11-101051071-CATGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051075_101051078del , CM000673.2:g.101051075_101051078del	GRCh38
NC_000011.9:g.100921806_100921809del , CM000673.1:g.100921806_100921809del	GRCh37
NC_000011.8:g.100427016_100427019del	NCBI36
NG_016475.1:g.83739_83742del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+349_2357+352del MANE Select	ENSP00000325120.5:n.2357+349_2357+352del
ENST00000263463.9:c.2051+349_2051+352del	ENSP00000263463.5:n.2051+349_2051+352del
ENST00000325455.9:c.2357+349_2357+352del	ENSP00000325120.5:n.2357+349_2357+352del
ENST00000526300.5:c.2051+349_2051+352del	ENSP00000436803.1:n.2051+349_2051+352del
ENST00000528960.5:c.2240+349_2240+352del	ENSP00000432914.1:n.2240+349_2240+352del
ENST00000530764.1:n.47+349_47+352del
ENST00000533207.5:n.1724+349_1724+352del
ENST00000534013.5:c.575+349_575+352del	ENSP00000436561.1:n.575+349_575+352del
ENST00000534780.5:c.2357+349_2357+352del	ENSP00000432352.1:n.2357+349_2357+352del
ENST00000617858.4:c.2052-126_2052-123del	ENSP00000481227.1:n.2052-126_2052-123del
ENST00000619228.2:c.2240+349_2240+352del	ENSP00000482698.1:n.2240+349_2240+352del
NM_000926.4:c.2357+349_2357+352del MANE Select	NP_000917.3:n.2357+349_2357+352del
NM_001202474.3:c.1865+349_1865+352del	NP_001189403.1:n.1865+349_1865+352del
NM_001271161.2:c.1559+349_1559+352del	NP_001258090.1:n.1559+349_1559+352del
NM_001271162.1:c.575+349_575+352del	NP_001258091.1:n.575+349_575+352del
NR_073141.2:n.2350+349_2350+352del
NR_073142.2:n.2233+349_2233+352del
NR_073143.2:n.2044+349_2044+352del
XM_006718858.2:c.2357+349_2357+352del	XP_006718921.1:n.2357+349_2357+352del
XM_006718858.3:c.2357+349_2357+352del	XP_006718921.1:n.2357+349_2357+352del
NM_001271162.2:c.575+349_575+352del	NP_001258091.1:n.575+349_575+352del
NR_073141.3:n.2364+349_2364+352del
NR_073142.3:n.2247+349_2247+352del
NR_073143.3:n.2058+349_2058+352del