Canonical Allele Identifier: CA2724859183
Gene: PGR HGNC NCBI

Linked Data

dbSNP Id: rs2135394398

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051658_101051659insATATTTTGTAGGGTAATAA , CM000673.2:g.101051658_101051659insATATTTTGTAGGGTAATAA GRCh38
NC_000011.9:g.100922389_100922390insATATTTTGTAGGGTAATAA , CM000673.1:g.100922389_100922390insATATTTTGTAGGGTAATAA GRCh37
NC_000011.8:g.100427599_100427600insATATTTTGTAGGGTAATAA NCBI36
NG_016475.1:g.83156_83157insTATTACCCTACAAAATATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2213-90_2213-89insTATTACCCTACAAAATATT MANE Select ENSP00000325120.5:n.2213-90_2213-89insTATTACCCTACAAAATATT
ENST00000263463.9:c.1907-90_1907-89insTATTACCCTACAAAATATT ENSP00000263463.5:n.1907-90_1907-89insTATTACCCTACAAAATATT
ENST00000325455.9:c.2213-90_2213-89insTATTACCCTACAAAATATT ENSP00000325120.5:n.2213-90_2213-89insTATTACCCTACAAAATATT
ENST00000526300.5:c.1907-90_1907-89insTATTACCCTACAAAATATT ENSP00000436803.1:n.1907-90_1907-89insTATTACCCTACAAAATATT
ENST00000528960.5:c.2096-90_2096-89insTATTACCCTACAAAATATT ENSP00000432914.1:n.2096-90_2096-89insTATTACCCTACAAAATATT
ENST00000533207.5:n.1580-90_1580-89insTATTACCCTACAAAATATT
ENST00000534013.5:c.431-90_431-89insTATTACCCTACAAAATATT ENSP00000436561.1:n.431-90_431-89insTATTACCCTACAAAATATT
ENST00000534780.5:c.2213-90_2213-89insTATTACCCTACAAAATATT ENSP00000432352.1:n.2213-90_2213-89insTATTACCCTACAAAATATT
ENST00000617858.4:c.1907-90_1907-89insTATTACCCTACAAAATATT ENSP00000481227.1:n.1907-90_1907-89insTATTACCCTACAAAATATT
ENST00000619228.2:c.2096-90_2096-89insTATTACCCTACAAAATATT ENSP00000482698.1:n.2096-90_2096-89insTATTACCCTACAAAATATT
NM_000926.4:c.2213-90_2213-89insTATTACCCTACAAAATATT MANE Select NP_000917.3:n.2213-90_2213-89insTATTACCCTACAAAATATT
NM_001202474.3:c.1721-90_1721-89insTATTACCCTACAAAATATT NP_001189403.1:n.1721-90_1721-89insTATTACCCTACAAAATATT
NM_001271161.2:c.1415-90_1415-89insTATTACCCTACAAAATATT NP_001258090.1:n.1415-90_1415-89insTATTACCCTACAAAATATT
NM_001271162.1:c.431-90_431-89insTATTACCCTACAAAATATT NP_001258091.1:n.431-90_431-89insTATTACCCTACAAAATATT
NR_073141.2:n.2206-90_2206-89insTATTACCCTACAAAATATT
NR_073142.2:n.2089-90_2089-89insTATTACCCTACAAAATATT
NR_073143.2:n.1900-90_1900-89insTATTACCCTACAAAATATT
XM_006718858.2:c.2213-90_2213-89insTATTACCCTACAAAATATT XP_006718921.1:n.2213-90_2213-89insTATTACCCTACAAAATATT
XR_947831.1:n.3894-90_3894-89insTATTACCCTACAAAATATT
XM_006718858.3:c.2213-90_2213-89insTATTACCCTACAAAATATT XP_006718921.1:n.2213-90_2213-89insTATTACCCTACAAAATATT
NM_001271162.2:c.431-90_431-89insTATTACCCTACAAAATATT NP_001258091.1:n.431-90_431-89insTATTACCCTACAAAATATT
NR_073141.3:n.2220-90_2220-89insTATTACCCTACAAAATATT
NR_073142.3:n.2103-90_2103-89insTATTACCCTACAAAATATT
NR_073143.3:n.1914-90_1914-89insTATTACCCTACAAAATATT