Canonical Allele Identifier: CA2724588208

Gene: PGR

Linked Data

• dbSNP Id: rs565892452

Genomic Alleles

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

Transcript Alleles

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