Canonical Allele Identifier: CA2793377563
Gene: PGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051666_101051667insCT , CM000673.2:g.101051666_101051667insCT GRCh38
NC_000011.9:g.100922397_100922398insCT , CM000673.1:g.100922397_100922398insCT GRCh37
NC_000011.8:g.100427607_100427608insCT NCBI36
NG_016475.1:g.83147_83148insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2213-99_2213-98insAG MANE Select ENSP00000325120.5:n.2213-99_2213-98insAG
ENST00000263463.9:c.1907-99_1907-98insAG ENSP00000263463.5:n.1907-99_1907-98insAG
ENST00000325455.9:c.2213-99_2213-98insAG ENSP00000325120.5:n.2213-99_2213-98insAG
ENST00000526300.5:c.1907-99_1907-98insAG ENSP00000436803.1:n.1907-99_1907-98insAG
ENST00000528960.5:c.2096-99_2096-98insAG ENSP00000432914.1:n.2096-99_2096-98insAG
ENST00000533207.5:n.1580-99_1580-98insAG
ENST00000534013.5:c.431-99_431-98insAG ENSP00000436561.1:n.431-99_431-98insAG
ENST00000534780.5:c.2213-99_2213-98insAG ENSP00000432352.1:n.2213-99_2213-98insAG
ENST00000617858.4:c.1907-99_1907-98insAG ENSP00000481227.1:n.1907-99_1907-98insAG
ENST00000619228.2:c.2096-99_2096-98insAG ENSP00000482698.1:n.2096-99_2096-98insAG
NM_000926.4:c.2213-99_2213-98insAG MANE Select NP_000917.3:n.2213-99_2213-98insAG
NM_001202474.3:c.1721-99_1721-98insAG NP_001189403.1:n.1721-99_1721-98insAG
NM_001271161.2:c.1415-99_1415-98insAG NP_001258090.1:n.1415-99_1415-98insAG
NM_001271162.1:c.431-99_431-98insAG NP_001258091.1:n.431-99_431-98insAG
NR_073141.2:n.2206-99_2206-98insAG
NR_073142.2:n.2089-99_2089-98insAG
NR_073143.2:n.1900-99_1900-98insAG
XM_006718858.2:c.2213-99_2213-98insAG XP_006718921.1:n.2213-99_2213-98insAG
XR_947831.1:n.3894-99_3894-98insAG
XM_006718858.3:c.2213-99_2213-98insAG XP_006718921.1:n.2213-99_2213-98insAG
NM_001271162.2:c.431-99_431-98insAG NP_001258091.1:n.431-99_431-98insAG
NR_073141.3:n.2220-99_2220-98insAG
NR_073142.3:n.2103-99_2103-98insAG
NR_073143.3:n.1914-99_1914-98insAG