Canonical Allele Identifier: CA2615658469

Gene: PGR

Linked Data

• gnomAD v4: 11-101034668-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034668C>A , CM000673.2:g.101034668C>A	GRCh38
NC_000011.9:g.100905399C>A , CM000673.1:g.100905399C>A	GRCh37
NC_000011.8:g.100410609C>A	NCBI36
NG_016475.1:g.100146G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4448G>T MANE Select	ENSP00000325120.5:n.*4448G>T
ENST00000325455.9:c.*4448G>T	ENSP00000325120.5:n.*4448G>T
NM_000926.4:c.*4448G>T MANE Select	NP_000917.3:n.*4448G>T
NM_001202474.3:c.*4448G>T	NP_001189403.1:n.*4448G>T
NM_001271161.2:c.*4448G>T	NP_001258090.1:n.*4448G>T
NM_001271162.1:c.*4448G>T	NP_001258091.1:n.*4448G>T
NR_073141.2:n.7191G>T
NR_073142.2:n.7074G>T
NR_073143.2:n.6806G>T
NM_001271162.2:c.*4448G>T	NP_001258091.1:n.*4448G>T
NR_073141.3:n.7205G>T
NR_073142.3:n.7088G>T
NR_073143.3:n.6820G>T