Canonical Allele Identifier: CA2793377291

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034821C>T , CM000673.2:g.101034821C>T	GRCh38
NC_000011.9:g.100905552C>T , CM000673.1:g.100905552C>T	GRCh37
NC_000011.8:g.100410762C>T	NCBI36
NG_016475.1:g.99993G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4295G>A MANE Select	ENSP00000325120.5:n.*4295G>A
ENST00000325455.9:c.*4295G>A	ENSP00000325120.5:n.*4295G>A
NM_000926.4:c.*4295G>A MANE Select	NP_000917.3:n.*4295G>A
NM_001202474.3:c.*4295G>A	NP_001189403.1:n.*4295G>A
NM_001271161.2:c.*4295G>A	NP_001258090.1:n.*4295G>A
NM_001271162.1:c.*4295G>A	NP_001258091.1:n.*4295G>A
NR_073141.2:n.7038G>A
NR_073142.2:n.6921G>A
NR_073143.2:n.6653G>A
NM_001271162.2:c.*4295G>A	NP_001258091.1:n.*4295G>A
NR_073141.3:n.7052G>A
NR_073142.3:n.6935G>A
NR_073143.3:n.6667G>A