Canonical Allele Identifier: CA2554318060

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050934_101050935del , CM000673.2:g.101050934_101050935del	GRCh38
NC_000011.9:g.100921665_100921666del , CM000673.1:g.100921665_100921666del	GRCh37
NC_000011.8:g.100426875_100426876del	NCBI36
NG_016475.1:g.83880_83881del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+490_2357+491del MANE Select	ENSP00000325120.5:n.2357+490_2357+491del
ENST00000263463.9:c.2051+490_2051+491del	ENSP00000263463.5:n.2051+490_2051+491del
ENST00000325455.9:c.2357+490_2357+491del	ENSP00000325120.5:n.2357+490_2357+491del
ENST00000526300.5:c.2051+490_2051+491del	ENSP00000436803.1:n.2051+490_2051+491del
ENST00000528960.5:c.2240+490_2240+491del	ENSP00000432914.1:n.2240+490_2240+491del
ENST00000530764.1:n.47+490_47+491del
ENST00000533207.5:n.1724+490_1724+491del
ENST00000534013.5:c.575+490_575+491del	ENSP00000436561.1:n.575+490_575+491del
ENST00000534780.5:c.2357+490_2357+491del	ENSP00000432352.1:n.2357+490_2357+491del
ENST00000617858.4:c.2052+15_2052+16del	ENSP00000481227.1:n.2052+15_2052+16del
ENST00000619228.2:c.2240+490_2240+491del	ENSP00000482698.1:n.2240+490_2240+491del
NM_000926.4:c.2357+490_2357+491del MANE Select	NP_000917.3:n.2357+490_2357+491del
NM_001202474.3:c.1865+490_1865+491del	NP_001189403.1:n.1865+490_1865+491del
NM_001271161.2:c.1559+490_1559+491del	NP_001258090.1:n.1559+490_1559+491del
NM_001271162.1:c.575+490_575+491del	NP_001258091.1:n.575+490_575+491del
NR_073141.2:n.2350+490_2350+491del
NR_073142.2:n.2233+490_2233+491del
NR_073143.2:n.2044+490_2044+491del
XM_006718858.2:c.2357+490_2357+491del	XP_006718921.1:n.2357+490_2357+491del
XM_006718858.3:c.2357+490_2357+491del	XP_006718921.1:n.2357+490_2357+491del
NM_001271162.2:c.575+490_575+491del	NP_001258091.1:n.575+490_575+491del
NR_073141.3:n.2364+490_2364+491del
NR_073142.3:n.2247+490_2247+491del
NR_073143.3:n.2058+490_2058+491del