Canonical Allele Identifier: CA670697033

Gene: PGR

Linked Data

• dbSNP Id: rs1247394991
• gnomAD v3: 11-101034405-AC-A
• gnomAD v4: 11-101034405-AC-A
• MyVariant Identifiers: chr11:g.100905137del (hg19) ; chr11:g.101034406del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034409del , CM000673.2:g.101034409del	GRCh38
NC_000011.9:g.100905140del , CM000673.1:g.100905140del	GRCh37
NC_000011.8:g.100410350del	NCBI36
NG_016475.1:g.100408del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.*4710del MANE Select	ENSP00000325120.5:n.*4710del
ENST00000325455.9:c.*4710del	ENSP00000325120.5:n.*4710del
NM_000926.4:c.*4710del MANE Select	NP_000917.3:n.*4710del
NM_001202474.3:c.*4710del	NP_001189403.1:n.*4710del
NM_001271161.2:c.*4710del	NP_001258090.1:n.*4710del
NM_001271162.1:c.*4710del	NP_001258091.1:n.*4710del
NR_073141.2:n.7453del
NR_073142.2:n.7336del
NR_073143.2:n.7068del
NM_001271162.2:c.*4710del	NP_001258091.1:n.*4710del
NR_073141.3:n.7467del
NR_073142.3:n.7350del
NR_073143.3:n.7082del