Canonical Allele Identifier: CA1995653874
Gene: PGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101062487C= , CM000673.2:g.101062487C= GRCh38
NC_000011.9:g.100933218C= , CM000673.1:g.100933218C= GRCh37
NC_000011.8:g.100438428C= NCBI36
NG_016475.1:g.72327G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2172G= MANE Select ENSP00000325120.5:p.Arg724=
ENST00000263463.9:c.1907-10919G= ENSP00000263463.5:n.1907-10919G=
ENST00000325455.9:c.2172G= ENSP00000325120.5:p.Arg724=
ENST00000526300.5:c.1907-10919G= ENSP00000436803.1:n.1907-10919G=
ENST00000528960.5:c.2055G= ENSP00000432914.1:p.Arg685=
ENST00000533207.5:n.1539G=
ENST00000534013.5:c.390G= ENSP00000436561.1:p.Arg130=
ENST00000534780.5:c.2172G= ENSP00000432352.1:p.Arg724=
ENST00000617858.4:c.1907-10919G= ENSP00000481227.1:n.1907-10919G=
ENST00000619228.2:c.2055G= ENSP00000482698.1:p.Arg685=
NM_000926.4:c.2172G= MANE Select NP_000917.3:p.Arg724=
NM_001202474.3:c.1680G= NP_001189403.1:p.Arg560=
NM_001271161.2:c.1415-10919G= NP_001258090.1:n.1415-10919G=
NM_001271162.1:c.390G= NP_001258091.1:p.Arg130=
NR_073141.2:n.2165G=
NR_073142.2:n.2048G=
NR_073143.2:n.1900-10919G=
XM_006718858.2:c.2172G= XP_006718921.1:p.Arg724=
XR_947831.1:n.3744G=
XM_006718858.3:c.2172G= XP_006718921.1:p.Arg724=
NM_001271162.2:c.390G= NP_001258091.1:p.Arg130=
NR_073141.3:n.2179G=
NR_073142.3:n.2062G=
NR_073143.3:n.1914-10919G=