Canonical Allele Identifier: CA2793377570

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051693_101051694insG , CM000673.2:g.101051693_101051694insG	GRCh38
NC_000011.9:g.100922424_100922425insG , CM000673.1:g.100922424_100922425insG	GRCh37
NC_000011.8:g.100427634_100427635insG	NCBI36
NG_016475.1:g.83120_83121insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2213-126_2213-125insC MANE Select	ENSP00000325120.5:n.2213-126_2213-125insC
ENST00000263463.9:c.1907-126_1907-125insC	ENSP00000263463.5:n.1907-126_1907-125insC
ENST00000325455.9:c.2213-126_2213-125insC	ENSP00000325120.5:n.2213-126_2213-125insC
ENST00000526300.5:c.1907-126_1907-125insC	ENSP00000436803.1:n.1907-126_1907-125insC
ENST00000528960.5:c.2096-126_2096-125insC	ENSP00000432914.1:n.2096-126_2096-125insC
ENST00000533207.5:n.1580-126_1580-125insC
ENST00000534013.5:c.431-126_431-125insC	ENSP00000436561.1:n.431-126_431-125insC
ENST00000534780.5:c.2213-126_2213-125insC	ENSP00000432352.1:n.2213-126_2213-125insC
ENST00000617858.4:c.1907-126_1907-125insC	ENSP00000481227.1:n.1907-126_1907-125insC
ENST00000619228.2:c.2096-126_2096-125insC	ENSP00000482698.1:n.2096-126_2096-125insC
NM_000926.4:c.2213-126_2213-125insC MANE Select	NP_000917.3:n.2213-126_2213-125insC
NM_001202474.3:c.1721-126_1721-125insC	NP_001189403.1:n.1721-126_1721-125insC
NM_001271161.2:c.1415-126_1415-125insC	NP_001258090.1:n.1415-126_1415-125insC
NM_001271162.1:c.431-126_431-125insC	NP_001258091.1:n.431-126_431-125insC
NR_073141.2:n.2206-126_2206-125insC
NR_073142.2:n.2089-126_2089-125insC
NR_073143.2:n.1900-126_1900-125insC
XM_006718858.2:c.2213-126_2213-125insC	XP_006718921.1:n.2213-126_2213-125insC
XR_947831.1:n.3894-126_3894-125insC
XM_006718858.3:c.2213-126_2213-125insC	XP_006718921.1:n.2213-126_2213-125insC
NM_001271162.2:c.431-126_431-125insC	NP_001258091.1:n.431-126_431-125insC
NR_073141.3:n.2220-126_2220-125insC
NR_073142.3:n.2103-126_2103-125insC
NR_073143.3:n.1914-126_1914-125insC