Canonical Allele Identifier: CA2615679565

Gene: PGR

Linked Data

• gnomAD v4: 11-101050926-CACTAGAACA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050928_101050936del , CM000673.2:g.101050928_101050936del	GRCh38
NC_000011.9:g.100921659_100921667del , CM000673.1:g.100921659_100921667del	GRCh37
NC_000011.8:g.100426869_100426877del	NCBI36
NG_016475.1:g.83879_83887del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+489_2357+497del MANE Select	ENSP00000325120.5:n.2357+489_2357+497del
ENST00000263463.9:c.2051+489_2051+497del	ENSP00000263463.5:n.2051+489_2051+497del
ENST00000325455.9:c.2357+489_2357+497del	ENSP00000325120.5:n.2357+489_2357+497del
ENST00000526300.5:c.2051+489_2051+497del	ENSP00000436803.1:n.2051+489_2051+497del
ENST00000528960.5:c.2240+489_2240+497del	ENSP00000432914.1:n.2240+489_2240+497del
ENST00000530764.1:n.47+489_47+497del
ENST00000533207.5:n.1724+489_1724+497del
ENST00000534013.5:c.575+489_575+497del	ENSP00000436561.1:n.575+489_575+497del
ENST00000534780.5:c.2357+489_2357+497del	ENSP00000432352.1:n.2357+489_2357+497del
ENST00000617858.4:c.2052+14_2052+22del	ENSP00000481227.1:n.2052+14_2052+22del
ENST00000619228.2:c.2240+489_2240+497del	ENSP00000482698.1:n.2240+489_2240+497del
NM_000926.4:c.2357+489_2357+497del MANE Select	NP_000917.3:n.2357+489_2357+497del
NM_001202474.3:c.1865+489_1865+497del	NP_001189403.1:n.1865+489_1865+497del
NM_001271161.2:c.1559+489_1559+497del	NP_001258090.1:n.1559+489_1559+497del
NM_001271162.1:c.575+489_575+497del	NP_001258091.1:n.575+489_575+497del
NR_073141.2:n.2350+489_2350+497del
NR_073142.2:n.2233+489_2233+497del
NR_073143.2:n.2044+489_2044+497del
XM_006718858.2:c.2357+489_2357+497del	XP_006718921.1:n.2357+489_2357+497del
XM_006718858.3:c.2357+489_2357+497del	XP_006718921.1:n.2357+489_2357+497del
NM_001271162.2:c.575+489_575+497del	NP_001258091.1:n.575+489_575+497del
NR_073141.3:n.2364+489_2364+497del
NR_073142.3:n.2247+489_2247+497del
NR_073143.3:n.2058+489_2058+497del