Canonical Allele Identifier: CA1995653819
Gene: PGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051051_101051055delinsAAATT , CM000673.2:g.101051051_101051055delinsAAATT GRCh38
NC_000011.9:g.100921782_100921786delinsAAATT , CM000673.1:g.100921782_100921786delinsAAATT GRCh37
NC_000011.8:g.100426992_100426996delinsAAATT NCBI36
NG_016475.1:g.83759_83763delinsAATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2357+369_2357+373delinsAATTT MANE Select ENSP00000325120.5:n.2357+369_2357+373delinsAATTT
ENST00000263463.9:c.2051+369_2051+373delinsAATTT ENSP00000263463.5:n.2051+369_2051+373delinsAATTT
ENST00000325455.9:c.2357+369_2357+373delinsAATTT ENSP00000325120.5:n.2357+369_2357+373delinsAATTT
ENST00000526300.5:c.2051+369_2051+373delinsAATTT ENSP00000436803.1:n.2051+369_2051+373delinsAATTT
ENST00000528960.5:c.2240+369_2240+373delinsAATTT ENSP00000432914.1:n.2240+369_2240+373delinsAATTT
ENST00000530764.1:n.47+369_47+373delinsAATTT
ENST00000533207.5:n.1724+369_1724+373delinsAATTT
ENST00000534013.5:c.575+369_575+373delinsAATTT ENSP00000436561.1:n.575+369_575+373delinsAATTT
ENST00000534780.5:c.2357+369_2357+373delinsAATTT ENSP00000432352.1:n.2357+369_2357+373delinsAATTT
ENST00000617858.4:c.2052-106_2052-102delinsAATTT ENSP00000481227.1:n.2052-106_2052-102delinsAATTT
ENST00000619228.2:c.2240+369_2240+373delinsAATTT ENSP00000482698.1:n.2240+369_2240+373delinsAATTT
NM_000926.4:c.2357+369_2357+373delinsAATTT MANE Select NP_000917.3:n.2357+369_2357+373delinsAATTT
NM_001202474.3:c.1865+369_1865+373delinsAATTT NP_001189403.1:n.1865+369_1865+373delinsAATTT
NM_001271161.2:c.1559+369_1559+373delinsAATTT NP_001258090.1:n.1559+369_1559+373delinsAATTT
NM_001271162.1:c.575+369_575+373delinsAATTT NP_001258091.1:n.575+369_575+373delinsAATTT
NR_073141.2:n.2350+369_2350+373delinsAATTT
NR_073142.2:n.2233+369_2233+373delinsAATTT
NR_073143.2:n.2044+369_2044+373delinsAATTT
XM_006718858.2:c.2357+369_2357+373delinsAATTT XP_006718921.1:n.2357+369_2357+373delinsAATTT
XM_006718858.3:c.2357+369_2357+373delinsAATTT XP_006718921.1:n.2357+369_2357+373delinsAATTT
NM_001271162.2:c.575+369_575+373delinsAATTT NP_001258091.1:n.575+369_575+373delinsAATTT
NR_073141.3:n.2364+369_2364+373delinsAATTT
NR_073142.3:n.2247+369_2247+373delinsAATTT
NR_073143.3:n.2058+369_2058+373delinsAATTT