Canonical Allele Identifier: CA2615658348

Gene: PGR

Linked Data

• gnomAD v4: 11-101034399-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034399G>T , CM000673.2:g.101034399G>T	GRCh38
NC_000011.9:g.100905130G>T , CM000673.1:g.100905130G>T	GRCh37
NC_000011.8:g.100410340G>T	NCBI36
NG_016475.1:g.100415C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4717C>A MANE Select	ENSP00000325120.5:n.*4717C>A
ENST00000325455.9:c.*4717C>A	ENSP00000325120.5:n.*4717C>A
NM_000926.4:c.*4717C>A MANE Select	NP_000917.3:n.*4717C>A
NM_001202474.3:c.*4717C>A	NP_001189403.1:n.*4717C>A
NM_001271161.2:c.*4717C>A	NP_001258090.1:n.*4717C>A
NM_001271162.1:c.*4717C>A	NP_001258091.1:n.*4717C>A
NR_073141.2:n.7460C>A
NR_073142.2:n.7343C>A
NR_073143.2:n.7075C>A
NM_001271162.2:c.*4717C>A	NP_001258091.1:n.*4717C>A
NR_073141.3:n.7474C>A
NR_073142.3:n.7357C>A
NR_073143.3:n.7089C>A