Canonical Allele Identifier: CA2503921236

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050936_101050937insGG , CM000673.2:g.101050936_101050937insGG	GRCh38
NC_000011.9:g.100921667_100921668insGG , CM000673.1:g.100921667_100921668insGG	GRCh37
NC_000011.8:g.100426877_100426878insGG	NCBI36
NG_016475.1:g.83877_83878insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+487_2357+488insCC MANE Select	ENSP00000325120.5:n.2357+487_2357+488insCC
ENST00000263463.9:c.2051+487_2051+488insCC	ENSP00000263463.5:n.2051+487_2051+488insCC
ENST00000325455.9:c.2357+487_2357+488insCC	ENSP00000325120.5:n.2357+487_2357+488insCC
ENST00000526300.5:c.2051+487_2051+488insCC	ENSP00000436803.1:n.2051+487_2051+488insCC
ENST00000528960.5:c.2240+487_2240+488insCC	ENSP00000432914.1:n.2240+487_2240+488insCC
ENST00000530764.1:n.47+487_47+488insCC
ENST00000533207.5:n.1724+487_1724+488insCC
ENST00000534013.5:c.575+487_575+488insCC	ENSP00000436561.1:n.575+487_575+488insCC
ENST00000534780.5:c.2357+487_2357+488insCC	ENSP00000432352.1:n.2357+487_2357+488insCC
ENST00000617858.4:c.2052+12_2052+13insCC	ENSP00000481227.1:n.2052+12_2052+13insCC
ENST00000619228.2:c.2240+487_2240+488insCC	ENSP00000482698.1:n.2240+487_2240+488insCC
NM_000926.4:c.2357+487_2357+488insCC MANE Select	NP_000917.3:n.2357+487_2357+488insCC
NM_001202474.3:c.1865+487_1865+488insCC	NP_001189403.1:n.1865+487_1865+488insCC
NM_001271161.2:c.1559+487_1559+488insCC	NP_001258090.1:n.1559+487_1559+488insCC
NM_001271162.1:c.575+487_575+488insCC	NP_001258091.1:n.575+487_575+488insCC
NR_073141.2:n.2350+487_2350+488insCC
NR_073142.2:n.2233+487_2233+488insCC
NR_073143.2:n.2044+487_2044+488insCC
XM_006718858.2:c.2357+487_2357+488insCC	XP_006718921.1:n.2357+487_2357+488insCC
XM_006718858.3:c.2357+487_2357+488insCC	XP_006718921.1:n.2357+487_2357+488insCC
NM_001271162.2:c.575+487_575+488insCC	NP_001258091.1:n.575+487_575+488insCC
NR_073141.3:n.2364+487_2364+488insCC
NR_073142.3:n.2247+487_2247+488insCC
NR_073143.3:n.2058+487_2058+488insCC