Canonical Allele Identifier: CA476499802

Gene: PGR

Linked Data

• dbSNP Id: rs1346787300
• gnomAD v2: 11-100905122-AAGG-A
• gnomAD v3: 11-101034391-AAGG-A
• gnomAD v4: 11-101034391-AAGG-A
• MyVariant Identifiers: chr11:g.100905123_100905125del (hg19) ; chr11:g.101034392_101034394del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034397_101034399del , CM000673.2:g.101034397_101034399del	GRCh38
NC_000011.9:g.100905128_100905130del , CM000673.1:g.100905128_100905130del	GRCh37
NC_000011.8:g.100410338_100410340del	NCBI36
NG_016475.1:g.100420_100422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4722_*4724del MANE Select	ENSP00000325120.5:n.*4722_*4724del
ENST00000325455.9:c.*4722_*4724del	ENSP00000325120.5:n.*4722_*4724del
NM_000926.4:c.*4722_*4724del MANE Select	NP_000917.3:n.*4722_*4724del
NM_001202474.3:c.*4722_*4724del	NP_001189403.1:n.*4722_*4724del
NM_001271161.2:c.*4722_*4724del	NP_001258090.1:n.*4722_*4724del
NM_001271162.1:c.*4722_*4724del	NP_001258091.1:n.*4722_*4724del
NR_073141.2:n.7465_7467del
NR_073142.2:n.7348_7350del
NR_073143.2:n.7080_7082del
NM_001271162.2:c.*4722_*4724del	NP_001258091.1:n.*4722_*4724del
NR_073141.3:n.7479_7481del
NR_073142.3:n.7362_7364del
NR_073143.3:n.7094_7096del