Canonical Allele Identifier: CA2615658347
Gene: PGR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034399G>A , CM000673.2:g.101034399G>A GRCh38
NC_000011.9:g.100905130G>A , CM000673.1:g.100905130G>A GRCh37
NC_000011.8:g.100410340G>A NCBI36
NG_016475.1:g.100415C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.*4717C>T MANE Select ENSP00000325120.5:n.*4717C>T
ENST00000325455.9:c.*4717C>T ENSP00000325120.5:n.*4717C>T
NM_000926.4:c.*4717C>T MANE Select NP_000917.3:n.*4717C>T
NM_001202474.3:c.*4717C>T NP_001189403.1:n.*4717C>T
NM_001271161.2:c.*4717C>T NP_001258090.1:n.*4717C>T
NM_001271162.1:c.*4717C>T NP_001258091.1:n.*4717C>T
NR_073141.2:n.7460C>T
NR_073142.2:n.7343C>T
NR_073143.2:n.7075C>T
NM_001271162.2:c.*4717C>T NP_001258091.1:n.*4717C>T
NR_073141.3:n.7474C>T
NR_073142.3:n.7357C>T
NR_073143.3:n.7089C>T