Canonical Allele Identifier: CA2615679907

Gene: PGR

Linked Data

• gnomAD v4: 11-101051493-AGAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051494_101051496del , CM000673.2:g.101051494_101051496del	GRCh38
NC_000011.9:g.100922225_100922227del , CM000673.1:g.100922225_100922227del	GRCh37
NC_000011.8:g.100427435_100427437del	NCBI36
NG_016475.1:g.83318_83320del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2285_2287del MANE Select	ENSP00000325120.5:p.Gly762_Leu763delinsVal
ENST00000263463.9:c.1979_1981del	ENSP00000263463.5:p.Gly660_Leu661delinsVal
ENST00000325455.9:c.2285_2287del	ENSP00000325120.5:p.Gly762_Leu763delinsVal
ENST00000526300.5:c.1979_1981del	ENSP00000436803.1:p.Gly660_Leu661delinsVal
ENST00000528960.5:c.2168_2170del	ENSP00000432914.1:p.Gly723_Leu724delinsVal
ENST00000533207.5:n.1652_1654del
ENST00000534013.5:c.503_505del	ENSP00000436561.1:p.Gly168_Leu169delinsVal
ENST00000534780.5:c.2285_2287del	ENSP00000432352.1:p.Gly762_Leu763delinsVal
ENST00000617858.4:c.1979_1981del	ENSP00000481227.1:p.Gly660_Leu661delinsVal
ENST00000619228.2:c.2168_2170del	ENSP00000482698.1:p.Gly723_Leu724delinsVal
NM_000926.4:c.2285_2287del MANE Select	NP_000917.3:p.Gly762_Leu763delinsVal
NM_001202474.3:c.1793_1795del	NP_001189403.1:p.Gly598_Leu599delinsVal
NM_001271161.2:c.1487_1489del	NP_001258090.1:p.Gly496_Leu497delinsVal
NM_001271162.1:c.503_505del	NP_001258091.1:p.Gly168_Leu169delinsVal
NR_073141.2:n.2278_2280del
NR_073142.2:n.2161_2163del
NR_073143.2:n.1972_1974del
XM_006718858.2:c.2285_2287del	XP_006718921.1:p.Gly762_Leu763delinsVal
XM_006718858.3:c.2285_2287del	XP_006718921.1:p.Gly762_Leu763delinsVal
NM_001271162.2:c.503_505del	NP_001258091.1:p.Gly168_Leu169delinsVal
NR_073141.3:n.2292_2294del
NR_073142.3:n.2175_2177del
NR_073143.3:n.1986_1988del