Canonical Allele Identifier: CA601422385

Gene: PGR

Linked Data

• dbSNP Id: rs1367365770
• gnomAD v2: 11-100905396-AG-A
• gnomAD v3: 11-101034665-AG-A
• gnomAD v4: 11-101034665-AG-A
• MyVariant Identifiers: chr11:g.100905397del (hg19) ; chr11:g.101034666del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034667del , CM000673.2:g.101034667del	GRCh38
NC_000011.9:g.100905398del , CM000673.1:g.100905398del	GRCh37
NC_000011.8:g.100410608del	NCBI36
NG_016475.1:g.100148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4450del MANE Select	ENSP00000325120.5:n.*4450del
ENST00000325455.9:c.*4450del	ENSP00000325120.5:n.*4450del
NM_000926.4:c.*4450del MANE Select	NP_000917.3:n.*4450del
NM_001202474.3:c.*4450del	NP_001189403.1:n.*4450del
NM_001271161.2:c.*4450del	NP_001258090.1:n.*4450del
NM_001271162.1:c.*4450del	NP_001258091.1:n.*4450del
NR_073141.2:n.7193del
NR_073142.2:n.7076del
NR_073143.2:n.6808del
NM_001271162.2:c.*4450del	NP_001258091.1:n.*4450del
NR_073141.3:n.7207del
NR_073142.3:n.7090del
NR_073143.3:n.6822del