Canonical Allele Identifier: CA2574957868

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051469_101051477del , CM000673.2:g.101051469_101051477del	GRCh38
NC_000011.9:g.100922200_100922208del , CM000673.1:g.100922200_100922208del	GRCh37
NC_000011.8:g.100427410_100427418del	NCBI36
NG_016475.1:g.83339_83347del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2306_2314del MANE Select	ENSP00000325120.5:p.Lys769_Val771del
ENST00000263463.9:c.2000_2008del	ENSP00000263463.5:p.Lys667_Val669del
ENST00000325455.9:c.2306_2314del	ENSP00000325120.5:p.Lys769_Val771del
ENST00000526300.5:c.2000_2008del	ENSP00000436803.1:p.Lys667_Val669del
ENST00000528960.5:c.2189_2197del	ENSP00000432914.1:p.Lys730_Val732del
ENST00000533207.5:n.1673_1681del
ENST00000534013.5:c.524_532del	ENSP00000436561.1:p.Lys175_Val177del
ENST00000534780.5:c.2306_2314del	ENSP00000432352.1:p.Lys769_Val771del
ENST00000617858.4:c.2000_2008del	ENSP00000481227.1:p.Lys667_Val669del
ENST00000619228.2:c.2189_2197del	ENSP00000482698.1:p.Lys730_Val732del
NM_000926.4:c.2306_2314del MANE Select	NP_000917.3:p.Lys769_Val771del
NM_001202474.3:c.1814_1822del	NP_001189403.1:p.Lys605_Val607del
NM_001271161.2:c.1508_1516del	NP_001258090.1:p.Lys503_Val505del
NM_001271162.1:c.524_532del	NP_001258091.1:p.Lys175_Val177del
NR_073141.2:n.2299_2307del
NR_073142.2:n.2182_2190del
NR_073143.2:n.1993_2001del
XM_006718858.2:c.2306_2314del	XP_006718921.1:p.Lys769_Val771del
XM_006718858.3:c.2306_2314del	XP_006718921.1:p.Lys769_Val771del
NM_001271162.2:c.524_532del	NP_001258091.1:p.Lys175_Val177del
NR_073141.3:n.2313_2321del
NR_073142.3:n.2196_2204del
NR_073143.3:n.2007_2015del