Canonical Allele Identifier: CA1995637130
Gene: PGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034501T= , CM000673.2:g.101034501T= GRCh38
NC_000011.9:g.100905232T= , CM000673.1:g.100905232T= GRCh37
NC_000011.8:g.100410442T= NCBI36
NG_016475.1:g.100313A=

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.*4615A= MANE Select ENSP00000325120.5:n.*4615A=
ENST00000325455.9:c.*4615A= ENSP00000325120.5:n.*4615A=
NM_000926.4:c.*4615A= MANE Select NP_000917.3:n.*4615A=
NM_001202474.3:c.*4615A= NP_001189403.1:n.*4615A=
NM_001271161.2:c.*4615A= NP_001258090.1:n.*4615A=
NM_001271162.1:c.*4615A= NP_001258091.1:n.*4615A=
NR_073141.2:n.7358A=
NR_073142.2:n.7241A=
NR_073143.2:n.6973A=
NM_001271162.2:c.*4615A= NP_001258091.1:n.*4615A=
NR_073141.3:n.7372A=
NR_073142.3:n.7255A=
NR_073143.3:n.6987A=