Canonical Allele Identifier: CA670697135

Gene: PGR

Linked Data

• dbSNP Id: rs1414396249
• MyVariant Identifiers: chr11:g.100905416del (hg19) ; chr11:g.101034685del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034685del , CM000673.2:g.101034685del	GRCh38
NC_000011.9:g.100905416del , CM000673.1:g.100905416del	GRCh37
NC_000011.8:g.100410626del	NCBI36
NG_016475.1:g.100129del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4431del MANE Select	ENSP00000325120.5:n.*4431del
ENST00000325455.9:c.*4431del	ENSP00000325120.5:n.*4431del
NM_000926.4:c.*4431del MANE Select	NP_000917.3:n.*4431del
NM_001202474.3:c.*4431del	NP_001189403.1:n.*4431del
NM_001271161.2:c.*4431del	NP_001258090.1:n.*4431del
NM_001271162.1:c.*4431del	NP_001258091.1:n.*4431del
NR_073141.2:n.7174del
NR_073142.2:n.7057del
NR_073143.2:n.6789del
NM_001271162.2:c.*4431del	NP_001258091.1:n.*4431del
NR_073141.3:n.7188del
NR_073142.3:n.7071del
NR_073143.3:n.6803del