Canonical Allele Identifier: CA670704987
Gene: PGR HGNC NCBI

Linked Data

dbSNP Id: rs1470410161

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051190_101051195del , CM000673.2:g.101051190_101051195del GRCh38
NC_000011.9:g.100921921_100921926del , CM000673.1:g.100921921_100921926del GRCh37
NC_000011.8:g.100427131_100427136del NCBI36
NG_016475.1:g.83623_83628del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2357+233_2357+238del MANE Select ENSP00000325120.5:n.2357+233_2357+238del
ENST00000263463.9:c.2051+233_2051+238del ENSP00000263463.5:n.2051+233_2051+238del
ENST00000325455.9:c.2357+233_2357+238del ENSP00000325120.5:n.2357+233_2357+238del
ENST00000526300.5:c.2051+233_2051+238del ENSP00000436803.1:n.2051+233_2051+238del
ENST00000528960.5:c.2240+233_2240+238del ENSP00000432914.1:n.2240+233_2240+238del
ENST00000530764.1:n.47+233_47+238del
ENST00000533207.5:n.1724+233_1724+238del
ENST00000534013.5:c.575+233_575+238del ENSP00000436561.1:n.575+233_575+238del
ENST00000534780.5:c.2357+233_2357+238del ENSP00000432352.1:n.2357+233_2357+238del
ENST00000617858.4:c.2051+233_2052-237del ENSP00000481227.1:n.2051+233_2052-237del
ENST00000619228.2:c.2240+233_2240+238del ENSP00000482698.1:n.2240+233_2240+238del
NM_000926.4:c.2357+233_2357+238del MANE Select NP_000917.3:n.2357+233_2357+238del
NM_001202474.3:c.1865+233_1865+238del NP_001189403.1:n.1865+233_1865+238del
NM_001271161.2:c.1559+233_1559+238del NP_001258090.1:n.1559+233_1559+238del
NM_001271162.1:c.575+233_575+238del NP_001258091.1:n.575+233_575+238del
NR_073141.2:n.2350+233_2350+238del
NR_073142.2:n.2233+233_2233+238del
NR_073143.2:n.2044+233_2044+238del
XM_006718858.2:c.2357+233_2357+238del XP_006718921.1:n.2357+233_2357+238del
XM_006718858.3:c.2357+233_2357+238del XP_006718921.1:n.2357+233_2357+238del
NM_001271162.2:c.575+233_575+238del NP_001258091.1:n.575+233_575+238del
NR_073141.3:n.2364+233_2364+238del
NR_073142.3:n.2247+233_2247+238del
NR_073143.3:n.2058+233_2058+238del