Canonical Allele Identifier: CA2615658351

Gene: PGR

Linked Data

• gnomAD v4: 11-101034402-C-A

Genomic Alleles

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

Transcript Alleles

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