Canonical Allele Identifier: CA2615658483

Gene: PGR

Linked Data

• gnomAD v4: 11-101034719-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034719A>G , CM000673.2:g.101034719A>G	GRCh38
NC_000011.9:g.100905450A>G , CM000673.1:g.100905450A>G	GRCh37
NC_000011.8:g.100410660A>G	NCBI36
NG_016475.1:g.100095T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4397T>C MANE Select	ENSP00000325120.5:n.*4397T>C
ENST00000325455.9:c.*4397T>C	ENSP00000325120.5:n.*4397T>C
NM_000926.4:c.*4397T>C MANE Select	NP_000917.3:n.*4397T>C
NM_001202474.3:c.*4397T>C	NP_001189403.1:n.*4397T>C
NM_001271161.2:c.*4397T>C	NP_001258090.1:n.*4397T>C
NM_001271162.1:c.*4397T>C	NP_001258091.1:n.*4397T>C
NR_073141.2:n.7140T>C
NR_073142.2:n.7023T>C
NR_073143.2:n.6755T>C
NM_001271162.2:c.*4397T>C	NP_001258091.1:n.*4397T>C
NR_073141.3:n.7154T>C
NR_073142.3:n.7037T>C
NR_073143.3:n.6769T>C