Canonical Allele Identifier: CA2615679567

Gene: PGR

Linked Data

• gnomAD v4: 11-101050927-A-AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050927_101050928insGT , CM000673.2:g.101050927_101050928insGT	GRCh38
NC_000011.9:g.100921658_100921659insGT , CM000673.1:g.100921658_100921659insGT	GRCh37
NC_000011.8:g.100426868_100426869insGT	NCBI36
NG_016475.1:g.83886_83887insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+496_2357+497insAC MANE Select	ENSP00000325120.5:n.2357+496_2357+497insAC
ENST00000263463.9:c.2051+496_2051+497insAC	ENSP00000263463.5:n.2051+496_2051+497insAC
ENST00000325455.9:c.2357+496_2357+497insAC	ENSP00000325120.5:n.2357+496_2357+497insAC
ENST00000526300.5:c.2051+496_2051+497insAC	ENSP00000436803.1:n.2051+496_2051+497insAC
ENST00000528960.5:c.2240+496_2240+497insAC	ENSP00000432914.1:n.2240+496_2240+497insAC
ENST00000530764.1:n.47+496_47+497insAC
ENST00000533207.5:n.1724+496_1724+497insAC
ENST00000534013.5:c.575+496_575+497insAC	ENSP00000436561.1:n.575+496_575+497insAC
ENST00000534780.5:c.2357+496_2357+497insAC	ENSP00000432352.1:n.2357+496_2357+497insAC
ENST00000617858.4:c.2052+21_2052+22insAC	ENSP00000481227.1:n.2052+21_2052+22insAC
ENST00000619228.2:c.2240+496_2240+497insAC	ENSP00000482698.1:n.2240+496_2240+497insAC
NM_000926.4:c.2357+496_2357+497insAC MANE Select	NP_000917.3:n.2357+496_2357+497insAC
NM_001202474.3:c.1865+496_1865+497insAC	NP_001189403.1:n.1865+496_1865+497insAC
NM_001271161.2:c.1559+496_1559+497insAC	NP_001258090.1:n.1559+496_1559+497insAC
NM_001271162.1:c.575+496_575+497insAC	NP_001258091.1:n.575+496_575+497insAC
NR_073141.2:n.2350+496_2350+497insAC
NR_073142.2:n.2233+496_2233+497insAC
NR_073143.2:n.2044+496_2044+497insAC
XM_006718858.2:c.2357+496_2357+497insAC	XP_006718921.1:n.2357+496_2357+497insAC
XM_006718858.3:c.2357+496_2357+497insAC	XP_006718921.1:n.2357+496_2357+497insAC
NM_001271162.2:c.575+496_575+497insAC	NP_001258091.1:n.575+496_575+497insAC
NR_073141.3:n.2364+496_2364+497insAC
NR_073142.3:n.2247+496_2247+497insAC
NR_073143.3:n.2058+496_2058+497insAC