Canonical Allele Identifier: CA2615680016
Gene: PGR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051720_101051723del , CM000673.2:g.101051720_101051723del GRCh38
NC_000011.9:g.100922451_100922454del , CM000673.1:g.100922451_100922454del GRCh37
NC_000011.8:g.100427661_100427664del NCBI36
NG_016475.1:g.83093_83096del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2213-153_2213-150del MANE Select ENSP00000325120.5:n.2213-153_2213-150del
ENST00000263463.9:c.1907-153_1907-150del ENSP00000263463.5:n.1907-153_1907-150del
ENST00000325455.9:c.2213-153_2213-150del ENSP00000325120.5:n.2213-153_2213-150del
ENST00000526300.5:c.1907-153_1907-150del ENSP00000436803.1:n.1907-153_1907-150del
ENST00000528960.5:c.2096-153_2096-150del ENSP00000432914.1:n.2096-153_2096-150del
ENST00000533207.5:n.1580-153_1580-150del
ENST00000534013.5:c.431-153_431-150del ENSP00000436561.1:n.431-153_431-150del
ENST00000534780.5:c.2213-153_2213-150del ENSP00000432352.1:n.2213-153_2213-150del
ENST00000617858.4:c.1907-153_1907-150del ENSP00000481227.1:n.1907-153_1907-150del
ENST00000619228.2:c.2096-153_2096-150del ENSP00000482698.1:n.2096-153_2096-150del
NM_000926.4:c.2213-153_2213-150del MANE Select NP_000917.3:n.2213-153_2213-150del
NM_001202474.3:c.1721-153_1721-150del NP_001189403.1:n.1721-153_1721-150del
NM_001271161.2:c.1415-153_1415-150del NP_001258090.1:n.1415-153_1415-150del
NM_001271162.1:c.431-153_431-150del NP_001258091.1:n.431-153_431-150del
NR_073141.2:n.2206-153_2206-150del
NR_073142.2:n.2089-153_2089-150del
NR_073143.2:n.1900-153_1900-150del
XM_006718858.2:c.2213-153_2213-150del XP_006718921.1:n.2213-153_2213-150del
XR_947831.1:n.3894-153_3894-150del
XM_006718858.3:c.2213-153_2213-150del XP_006718921.1:n.2213-153_2213-150del
NM_001271162.2:c.431-153_431-150del NP_001258091.1:n.431-153_431-150del
NR_073141.3:n.2220-153_2220-150del
NR_073142.3:n.2103-153_2103-150del
NR_073143.3:n.1914-153_1914-150del