Canonical Allele Identifier: CA2615658501

Gene: PGR

Linked Data

• gnomAD v4: 11-101034782-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034783dup , CM000673.2:g.101034783dup	GRCh38
NC_000011.9:g.100905514dup , CM000673.1:g.100905514dup	GRCh37
NC_000011.8:g.100410724dup	NCBI36
NG_016475.1:g.100031dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4333dup MANE Select	ENSP00000325120.5:n.*4333dup
ENST00000325455.9:c.*4333dup	ENSP00000325120.5:n.*4333dup
NM_000926.4:c.*4333dup MANE Select	NP_000917.3:n.*4333dup
NM_001202474.3:c.*4333dup	NP_001189403.1:n.*4333dup
NM_001271161.2:c.*4333dup	NP_001258090.1:n.*4333dup
NM_001271162.1:c.*4333dup	NP_001258091.1:n.*4333dup
NR_073141.2:n.7076dup
NR_073142.2:n.6959dup
NR_073143.2:n.6691dup
NM_001271162.2:c.*4333dup	NP_001258091.1:n.*4333dup
NR_073141.3:n.7090dup
NR_073142.3:n.6973dup
NR_073143.3:n.6705dup