Canonical Allele Identifier: CA2615658513

Gene: PGR

Linked Data

• gnomAD v4: 11-101034821-C-A

Genomic Alleles

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

Transcript Alleles

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