Canonical Allele Identifier: CA1995654421
Gene: PGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051426A= , CM000673.2:g.101051426A= GRCh38
NC_000011.9:g.100922157A= , CM000673.1:g.100922157A= GRCh37
NC_000011.8:g.100427367A= NCBI36
NG_016475.1:g.83388T=

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.2355T= MANE Select ENSP00000325120.5:p.Asn785=
ENST00000263463.9:c.2049T= ENSP00000263463.5:p.Asn683=
ENST00000325455.9:c.2355T= ENSP00000325120.5:p.Asn785=
ENST00000526300.5:c.2049T= ENSP00000436803.1:p.Asn683=
ENST00000528960.5:c.2238T= ENSP00000432914.1:p.Asn746=
ENST00000530764.1:n.45T=
ENST00000533207.5:n.1722T=
ENST00000534013.5:c.573T= ENSP00000436561.1:p.Asn191=
ENST00000534780.5:c.2355T= ENSP00000432352.1:p.Asn785=
ENST00000617858.4:c.2049T= ENSP00000481227.1:p.Asn683=
ENST00000619228.2:c.2238T= ENSP00000482698.1:p.Asn746=
NM_000926.4:c.2355T= MANE Select NP_000917.3:p.Asn785=
NM_001202474.3:c.1863T= NP_001189403.1:p.Asn621=
NM_001271161.2:c.1557T= NP_001258090.1:p.Asn519=
NM_001271162.1:c.573T= NP_001258091.1:p.Asn191=
NR_073141.2:n.2348T=
NR_073142.2:n.2231T=
NR_073143.2:n.2042T=
XM_006718858.2:c.2355T= XP_006718921.1:p.Asn785=
XM_006718858.3:c.2355T= XP_006718921.1:p.Asn785=
NM_001271162.2:c.573T= NP_001258091.1:p.Asn191=
NR_073141.3:n.2362T=
NR_073142.3:n.2245T=
NR_073143.3:n.2056T=