Canonical Allele Identifier: CA6243479

Gene: PGR

Linked Data

• dbSNP Id: rs567769039
• ExAC: 11:100921641 CT / C
• gnomAD v2: 11-100921641-CT-C
• gnomAD v3: 11-101050910-CT-C
• gnomAD v4: 11-101050910-CT-C
• MyVariant Identifiers: chr11:g.100921642del (hg19) ; chr11:g.101050911del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050911del , CM000673.2:g.101050911del	GRCh38
NC_000011.9:g.100921642del , CM000673.1:g.100921642del	GRCh37
NC_000011.8:g.100426852del	NCBI36
NG_016475.1:g.83903del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+513del MANE Select	ENSP00000325120.5:n.2357+513del
ENST00000263463.9:c.2051+513del	ENSP00000263463.5:n.2051+513del
ENST00000325455.9:c.2357+513del	ENSP00000325120.5:n.2357+513del
ENST00000526300.5:c.2051+513del	ENSP00000436803.1:n.2051+513del
ENST00000528960.5:c.2240+513del	ENSP00000432914.1:n.2240+513del
ENST00000530764.1:n.47+513del
ENST00000533207.5:n.1724+513del
ENST00000534013.5:c.575+513del	ENSP00000436561.1:n.575+513del
ENST00000534780.5:c.2357+513del	ENSP00000432352.1:n.2357+513del
ENST00000617858.4:c.2052+38del	ENSP00000481227.1:n.2052+38del
ENST00000619228.2:c.2240+513del	ENSP00000482698.1:n.2240+513del
NM_000926.4:c.2357+513del MANE Select	NP_000917.3:n.2357+513del
NM_001202474.3:c.1865+513del	NP_001189403.1:n.1865+513del
NM_001271161.2:c.1559+513del	NP_001258090.1:n.1559+513del
NM_001271162.1:c.575+513del	NP_001258091.1:n.575+513del
NR_073141.2:n.2350+513del
NR_073142.2:n.2233+513del
NR_073143.2:n.2044+513del
XM_006718858.2:c.2357+513del	XP_006718921.1:n.2357+513del
XM_006718858.3:c.2357+513del	XP_006718921.1:n.2357+513del
NM_001271162.2:c.575+513del	NP_001258091.1:n.575+513del
NR_073141.3:n.2364+513del
NR_073142.3:n.2247+513del
NR_073143.3:n.2058+513del