Canonical Allele Identifier: CA2615658357

Gene: PGR

Linked Data

• gnomAD v4: 11-101034411-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034413del , CM000673.2:g.101034413del	GRCh38
NC_000011.9:g.100905144del , CM000673.1:g.100905144del	GRCh37
NC_000011.8:g.100410354del	NCBI36
NG_016475.1:g.100402del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.*4704del MANE Select	ENSP00000325120.5:n.*4704del
ENST00000325455.9:c.*4704del	ENSP00000325120.5:n.*4704del
NM_000926.4:c.*4704del MANE Select	NP_000917.3:n.*4704del
NM_001202474.3:c.*4704del	NP_001189403.1:n.*4704del
NM_001271161.2:c.*4704del	NP_001258090.1:n.*4704del
NM_001271162.1:c.*4704del	NP_001258091.1:n.*4704del
NR_073141.2:n.7447del
NR_073142.2:n.7330del
NR_073143.2:n.7062del
NM_001271162.2:c.*4704del	NP_001258091.1:n.*4704del
NR_073141.3:n.7461del
NR_073142.3:n.7344del
NR_073143.3:n.7076del