Canonical Allele Identifier: CA670704945
Gene: PGR HGNC NCBI

Linked Data

dbSNP Id: rs1441963184

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051111_101051114del , CM000673.2:g.101051111_101051114del GRCh38
NC_000011.9:g.100921842_100921845del , CM000673.1:g.100921842_100921845del GRCh37
NC_000011.8:g.100427052_100427055del NCBI36
NG_016475.1:g.83703_83706del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2357+313_2357+316del MANE Select ENSP00000325120.5:n.2357+313_2357+316del
ENST00000263463.9:c.2051+313_2051+316del ENSP00000263463.5:n.2051+313_2051+316del
ENST00000325455.9:c.2357+313_2357+316del ENSP00000325120.5:n.2357+313_2357+316del
ENST00000526300.5:c.2051+313_2051+316del ENSP00000436803.1:n.2051+313_2051+316del
ENST00000528960.5:c.2240+313_2240+316del ENSP00000432914.1:n.2240+313_2240+316del
ENST00000530764.1:n.47+313_47+316del
ENST00000533207.5:n.1724+313_1724+316del
ENST00000534013.5:c.575+313_575+316del ENSP00000436561.1:n.575+313_575+316del
ENST00000534780.5:c.2357+313_2357+316del ENSP00000432352.1:n.2357+313_2357+316del
ENST00000617858.4:c.2052-162_2052-159del ENSP00000481227.1:n.2052-162_2052-159del
ENST00000619228.2:c.2240+313_2240+316del ENSP00000482698.1:n.2240+313_2240+316del
NM_000926.4:c.2357+313_2357+316del MANE Select NP_000917.3:n.2357+313_2357+316del
NM_001202474.3:c.1865+313_1865+316del NP_001189403.1:n.1865+313_1865+316del
NM_001271161.2:c.1559+313_1559+316del NP_001258090.1:n.1559+313_1559+316del
NM_001271162.1:c.575+313_575+316del NP_001258091.1:n.575+313_575+316del
NR_073141.2:n.2350+313_2350+316del
NR_073142.2:n.2233+313_2233+316del
NR_073143.2:n.2044+313_2044+316del
XM_006718858.2:c.2357+313_2357+316del XP_006718921.1:n.2357+313_2357+316del
XM_006718858.3:c.2357+313_2357+316del XP_006718921.1:n.2357+313_2357+316del
NM_001271162.2:c.575+313_575+316del NP_001258091.1:n.575+313_575+316del
NR_073141.3:n.2364+313_2364+316del
NR_073142.3:n.2247+313_2247+316del
NR_073143.3:n.2058+313_2058+316del