Canonical Allele Identifier: CA2615658352

Gene: PGR

Linked Data

• gnomAD v4: 11-101034402-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034402C>T , CM000673.2:g.101034402C>T	GRCh38
NC_000011.9:g.100905133C>T , CM000673.1:g.100905133C>T	GRCh37
NC_000011.8:g.100410343C>T	NCBI36
NG_016475.1:g.100412G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.*4714G>A MANE Select	ENSP00000325120.5:n.*4714G>A
ENST00000325455.9:c.*4714G>A	ENSP00000325120.5:n.*4714G>A
NM_000926.4:c.*4714G>A MANE Select	NP_000917.3:n.*4714G>A
NM_001202474.3:c.*4714G>A	NP_001189403.1:n.*4714G>A
NM_001271161.2:c.*4714G>A	NP_001258090.1:n.*4714G>A
NM_001271162.1:c.*4714G>A	NP_001258091.1:n.*4714G>A
NR_073141.2:n.7457G>A
NR_073142.2:n.7340G>A
NR_073143.2:n.7072G>A
NM_001271162.2:c.*4714G>A	NP_001258091.1:n.*4714G>A
NR_073141.3:n.7471G>A
NR_073142.3:n.7354G>A
NR_073143.3:n.7086G>A