Canonical Allele Identifier: CA2574957867

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051429_101051432dup , CM000673.2:g.101051429_101051432dup	GRCh38
NC_000011.9:g.100922160_100922163dup , CM000673.1:g.100922160_100922163dup	GRCh37
NC_000011.8:g.100427370_100427373dup	NCBI36
NG_016475.1:g.83383_83386dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2350_2353dup MANE Select	ENSP00000325120.5:p.Asn785ThrfsTer3
ENST00000263463.9:c.2044_2047dup	ENSP00000263463.5:p.Asn683ThrfsTer3
ENST00000325455.9:c.2350_2353dup	ENSP00000325120.5:p.Asn785ThrfsTer3
ENST00000526300.5:c.2044_2047dup	ENSP00000436803.1:p.Asn683ThrfsTer3
ENST00000528960.5:c.2233_2236dup	ENSP00000432914.1:p.Asn746ThrfsTer3
ENST00000530764.1:n.40_43dup
ENST00000533207.5:n.1717_1720dup
ENST00000534013.5:c.568_571dup	ENSP00000436561.1:p.Asn191ThrfsTer3
ENST00000534780.5:c.2350_2353dup	ENSP00000432352.1:p.Asn785ThrfsTer3
ENST00000617858.4:c.2044_2047dup	ENSP00000481227.1:p.Asn683ThrfsTer3
ENST00000619228.2:c.2233_2236dup	ENSP00000482698.1:p.Asn746ThrfsTer3
NM_000926.4:c.2350_2353dup MANE Select	NP_000917.3:p.Asn785ThrfsTer3
NM_001202474.3:c.1858_1861dup	NP_001189403.1:p.Asn621ThrfsTer3
NM_001271161.2:c.1552_1555dup	NP_001258090.1:p.Asn519ThrfsTer3
NM_001271162.1:c.568_571dup	NP_001258091.1:p.Asn191ThrfsTer3
NR_073141.2:n.2343_2346dup
NR_073142.2:n.2226_2229dup
NR_073143.2:n.2037_2040dup
XM_006718858.2:c.2350_2353dup	XP_006718921.1:p.Asn785ThrfsTer3
XM_006718858.3:c.2350_2353dup	XP_006718921.1:p.Asn785ThrfsTer3
NM_001271162.2:c.568_571dup	NP_001258091.1:p.Asn191ThrfsTer3
NR_073141.3:n.2357_2360dup
NR_073142.3:n.2240_2243dup
NR_073143.3:n.2051_2054dup