Canonical Allele Identifier: CA227513631

Gene: PGR

Linked Data

• dbSNP Id: rs565892452
• gnomAD v2: 11-100905133-C-CA
• gnomAD v3: 11-101034402-C-CA
• gnomAD v4: 11-101034402-C-CA
• MyVariant Identifiers: chr11:g.100905133_100905134insA (hg19) ; chr11:g.101034402_101034403insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034405dup , CM000673.2:g.101034405dup	GRCh38
NC_000011.9:g.100905136dup , CM000673.1:g.100905136dup	GRCh37
NC_000011.8:g.100410346dup	NCBI36
NG_016475.1:g.100411dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.*4713dup MANE Select	ENSP00000325120.5:n.*4713dup
ENST00000325455.9:c.*4713dup	ENSP00000325120.5:n.*4713dup
NM_000926.4:c.*4713dup MANE Select	NP_000917.3:n.*4713dup
NM_001202474.3:c.*4713dup	NP_001189403.1:n.*4713dup
NM_001271161.2:c.*4713dup	NP_001258090.1:n.*4713dup
NM_001271162.1:c.*4713dup	NP_001258091.1:n.*4713dup
NR_073141.2:n.7456dup
NR_073142.2:n.7339dup
NR_073143.2:n.7071dup
NM_001271162.2:c.*4713dup	NP_001258091.1:n.*4713dup
NR_073141.3:n.7470dup
NR_073142.3:n.7353dup
NR_073143.3:n.7085dup