Canonical Allele Identifier: CA2615658362

Gene: PGR

Linked Data

• gnomAD v4: 11-101034421-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034421C>A , CM000673.2:g.101034421C>A	GRCh38
NC_000011.9:g.100905152C>A , CM000673.1:g.100905152C>A	GRCh37
NC_000011.8:g.100410362C>A	NCBI36
NG_016475.1:g.100393G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4695G>T MANE Select	ENSP00000325120.5:n.*4695G>T
ENST00000325455.9:c.*4695G>T	ENSP00000325120.5:n.*4695G>T
NM_000926.4:c.*4695G>T MANE Select	NP_000917.3:n.*4695G>T
NM_001202474.3:c.*4695G>T	NP_001189403.1:n.*4695G>T
NM_001271161.2:c.*4695G>T	NP_001258090.1:n.*4695G>T
NM_001271162.1:c.*4695G>T	NP_001258091.1:n.*4695G>T
NR_073141.2:n.7438G>T
NR_073142.2:n.7321G>T
NR_073143.2:n.7053G>T
NM_001271162.2:c.*4695G>T	NP_001258091.1:n.*4695G>T
NR_073141.3:n.7452G>T
NR_073142.3:n.7335G>T
NR_073143.3:n.7067G>T