Canonical Allele Identifier: CA941519541
Gene: PGR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051672_101051673insT , CM000673.2:g.101051672_101051673insT GRCh38
NC_000011.9:g.100922403_100922404insT , CM000673.1:g.100922403_100922404insT GRCh37
NC_000011.8:g.100427613_100427614insT NCBI36
NG_016475.1:g.83141_83142insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2213-105_2213-104insA MANE Select ENSP00000325120.5:n.2213-105_2213-104insA
ENST00000263463.9:c.1907-105_1907-104insA ENSP00000263463.5:n.1907-105_1907-104insA
ENST00000325455.9:c.2213-105_2213-104insA ENSP00000325120.5:n.2213-105_2213-104insA
ENST00000526300.5:c.1907-105_1907-104insA ENSP00000436803.1:n.1907-105_1907-104insA
ENST00000528960.5:c.2096-105_2096-104insA ENSP00000432914.1:n.2096-105_2096-104insA
ENST00000533207.5:n.1580-105_1580-104insA
ENST00000534013.5:c.431-105_431-104insA ENSP00000436561.1:n.431-105_431-104insA
ENST00000534780.5:c.2213-105_2213-104insA ENSP00000432352.1:n.2213-105_2213-104insA
ENST00000617858.4:c.1907-105_1907-104insA ENSP00000481227.1:n.1907-105_1907-104insA
ENST00000619228.2:c.2096-105_2096-104insA ENSP00000482698.1:n.2096-105_2096-104insA
NM_000926.4:c.2213-105_2213-104insA MANE Select NP_000917.3:n.2213-105_2213-104insA
NM_001202474.3:c.1721-105_1721-104insA NP_001189403.1:n.1721-105_1721-104insA
NM_001271161.2:c.1415-105_1415-104insA NP_001258090.1:n.1415-105_1415-104insA
NM_001271162.1:c.431-105_431-104insA NP_001258091.1:n.431-105_431-104insA
NR_073141.2:n.2206-105_2206-104insA
NR_073142.2:n.2089-105_2089-104insA
NR_073143.2:n.1900-105_1900-104insA
XM_006718858.2:c.2213-105_2213-104insA XP_006718921.1:n.2213-105_2213-104insA
XR_947831.1:n.3894-105_3894-104insA
XM_006718858.3:c.2213-105_2213-104insA XP_006718921.1:n.2213-105_2213-104insA
NM_001271162.2:c.431-105_431-104insA NP_001258091.1:n.431-105_431-104insA
NR_073141.3:n.2220-105_2220-104insA
NR_073142.3:n.2103-105_2103-104insA
NR_073143.3:n.1914-105_1914-104insA