Canonical Allele Identifier: CA1995637163

Gene: PGR

Linked Data

• dbSNP Id: rs1859450127

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034584dup , CM000673.2:g.101034584dup	GRCh38
NC_000011.9:g.100905315dup , CM000673.1:g.100905315dup	GRCh37
NC_000011.8:g.100410525dup	NCBI36
NG_016475.1:g.100233dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4535dup MANE Select	ENSP00000325120.5:n.*4535dup
ENST00000325455.9:c.*4535dup	ENSP00000325120.5:n.*4535dup
NM_000926.4:c.*4535dup MANE Select	NP_000917.3:n.*4535dup
NM_001202474.3:c.*4535dup	NP_001189403.1:n.*4535dup
NM_001271161.2:c.*4535dup	NP_001258090.1:n.*4535dup
NM_001271162.1:c.*4535dup	NP_001258091.1:n.*4535dup
NR_073141.2:n.7278dup
NR_073142.2:n.7161dup
NR_073143.2:n.6893dup
NM_001271162.2:c.*4535dup	NP_001258091.1:n.*4535dup
NR_073141.3:n.7292dup
NR_073142.3:n.7175dup
NR_073143.3:n.6907dup