Canonical Allele Identifier: CA2615658443

Gene: PGR

Linked Data

• gnomAD v4: 11-101034575-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034575T>G , CM000673.2:g.101034575T>G	GRCh38
NC_000011.9:g.100905306T>G , CM000673.1:g.100905306T>G	GRCh37
NC_000011.8:g.100410516T>G	NCBI36
NG_016475.1:g.100239A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4541A>C MANE Select	ENSP00000325120.5:n.*4541A>C
ENST00000325455.9:c.*4541A>C	ENSP00000325120.5:n.*4541A>C
NM_000926.4:c.*4541A>C MANE Select	NP_000917.3:n.*4541A>C
NM_001202474.3:c.*4541A>C	NP_001189403.1:n.*4541A>C
NM_001271161.2:c.*4541A>C	NP_001258090.1:n.*4541A>C
NM_001271162.1:c.*4541A>C	NP_001258091.1:n.*4541A>C
NR_073141.2:n.7284A>C
NR_073142.2:n.7167A>C
NR_073143.2:n.6899A>C
NM_001271162.2:c.*4541A>C	NP_001258091.1:n.*4541A>C
NR_073141.3:n.7298A>C
NR_073142.3:n.7181A>C
NR_073143.3:n.6913A>C