Canonical Allele Identifier: CA1995653884
Gene: PGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101062497A= , CM000673.2:g.101062497A= GRCh38
NC_000011.9:g.100933228A= , CM000673.1:g.100933228A= GRCh37
NC_000011.8:g.100438438A= NCBI36
NG_016475.1:g.72317T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2162T= MANE Select ENSP00000325120.5:p.Leu721=
ENST00000263463.9:c.1907-10929T= ENSP00000263463.5:n.1907-10929T=
ENST00000325455.9:c.2162T= ENSP00000325120.5:p.Leu721=
ENST00000526300.5:c.1907-10929T= ENSP00000436803.1:n.1907-10929T=
ENST00000528960.5:c.2045T= ENSP00000432914.1:p.Leu682=
ENST00000533207.5:n.1529T=
ENST00000534013.5:c.380T= ENSP00000436561.1:p.Leu127=
ENST00000534780.5:c.2162T= ENSP00000432352.1:p.Leu721=
ENST00000617858.4:c.1907-10929T= ENSP00000481227.1:n.1907-10929T=
ENST00000619228.2:c.2045T= ENSP00000482698.1:p.Leu682=
NM_000926.4:c.2162T= MANE Select NP_000917.3:p.Leu721=
NM_001202474.3:c.1670T= NP_001189403.1:p.Leu557=
NM_001271161.2:c.1415-10929T= NP_001258090.1:n.1415-10929T=
NM_001271162.1:c.380T= NP_001258091.1:p.Leu127=
NR_073141.2:n.2155T=
NR_073142.2:n.2038T=
NR_073143.2:n.1900-10929T=
XM_006718858.2:c.2162T= XP_006718921.1:p.Leu721=
XR_947831.1:n.3734T=
XM_006718858.3:c.2162T= XP_006718921.1:p.Leu721=
NM_001271162.2:c.380T= NP_001258091.1:p.Leu127=
NR_073141.3:n.2169T=
NR_073142.3:n.2052T=
NR_073143.3:n.1914-10929T=