Canonical Allele Identifier: CA2615658402
Gene: PGR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034516_101034533del , CM000673.2:g.101034516_101034533del GRCh38
NC_000011.9:g.100905247_100905264del , CM000673.1:g.100905247_100905264del GRCh37
NC_000011.8:g.100410457_100410474del NCBI36
NG_016475.1:g.100282_100299del

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.*4584_*4601del MANE Select ENSP00000325120.5:n.*4584_*4601del
ENST00000325455.9:c.*4584_*4601del ENSP00000325120.5:n.*4584_*4601del
NM_000926.4:c.*4584_*4601del MANE Select NP_000917.3:n.*4584_*4601del
NM_001202474.3:c.*4584_*4601del NP_001189403.1:n.*4584_*4601del
NM_001271161.2:c.*4584_*4601del NP_001258090.1:n.*4584_*4601del
NM_001271162.1:c.*4584_*4601del NP_001258091.1:n.*4584_*4601del
NR_073141.2:n.7327_7344del
NR_073142.2:n.7210_7227del
NR_073143.2:n.6942_6959del
NM_001271162.2:c.*4584_*4601del NP_001258091.1:n.*4584_*4601del
NR_073141.3:n.7341_7358del
NR_073142.3:n.7224_7241del
NR_073143.3:n.6956_6973del