Canonical Allele Identifier: CA2615658419
Gene: PGR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034546_101034551del , CM000673.2:g.101034546_101034551del GRCh38
NC_000011.9:g.100905277_100905282del , CM000673.1:g.100905277_100905282del GRCh37
NC_000011.8:g.100410487_100410492del NCBI36
NG_016475.1:g.100263_100268del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.*4565_*4570del MANE Select ENSP00000325120.5:n.*4565_*4570del
ENST00000325455.9:c.*4565_*4570del ENSP00000325120.5:n.*4565_*4570del
NM_000926.4:c.*4565_*4570del MANE Select NP_000917.3:n.*4565_*4570del
NM_001202474.3:c.*4565_*4570del NP_001189403.1:n.*4565_*4570del
NM_001271161.2:c.*4565_*4570del NP_001258090.1:n.*4565_*4570del
NM_001271162.1:c.*4565_*4570del NP_001258091.1:n.*4565_*4570del
NR_073141.2:n.7308_7313del
NR_073142.2:n.7191_7196del
NR_073143.2:n.6923_6928del
NM_001271162.2:c.*4565_*4570del NP_001258091.1:n.*4565_*4570del
NR_073141.3:n.7322_7327del
NR_073142.3:n.7205_7210del
NR_073143.3:n.6937_6942del