Canonical Allele Identifier: CA2793377573

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051704_101051705insT , CM000673.2:g.101051704_101051705insT	GRCh38
NC_000011.9:g.100922435_100922436insT , CM000673.1:g.100922435_100922436insT	GRCh37
NC_000011.8:g.100427645_100427646insT	NCBI36
NG_016475.1:g.83109_83110insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2213-137_2213-136insA MANE Select	ENSP00000325120.5:n.2213-137_2213-136insA
ENST00000263463.9:c.1907-137_1907-136insA	ENSP00000263463.5:n.1907-137_1907-136insA
ENST00000325455.9:c.2213-137_2213-136insA	ENSP00000325120.5:n.2213-137_2213-136insA
ENST00000526300.5:c.1907-137_1907-136insA	ENSP00000436803.1:n.1907-137_1907-136insA
ENST00000528960.5:c.2096-137_2096-136insA	ENSP00000432914.1:n.2096-137_2096-136insA
ENST00000533207.5:n.1580-137_1580-136insA
ENST00000534013.5:c.431-137_431-136insA	ENSP00000436561.1:n.431-137_431-136insA
ENST00000534780.5:c.2213-137_2213-136insA	ENSP00000432352.1:n.2213-137_2213-136insA
ENST00000617858.4:c.1907-137_1907-136insA	ENSP00000481227.1:n.1907-137_1907-136insA
ENST00000619228.2:c.2096-137_2096-136insA	ENSP00000482698.1:n.2096-137_2096-136insA
NM_000926.4:c.2213-137_2213-136insA MANE Select	NP_000917.3:n.2213-137_2213-136insA
NM_001202474.3:c.1721-137_1721-136insA	NP_001189403.1:n.1721-137_1721-136insA
NM_001271161.2:c.1415-137_1415-136insA	NP_001258090.1:n.1415-137_1415-136insA
NM_001271162.1:c.431-137_431-136insA	NP_001258091.1:n.431-137_431-136insA
NR_073141.2:n.2206-137_2206-136insA
NR_073142.2:n.2089-137_2089-136insA
NR_073143.2:n.1900-137_1900-136insA
XM_006718858.2:c.2213-137_2213-136insA	XP_006718921.1:n.2213-137_2213-136insA
XR_947831.1:n.3894-137_3894-136insA
XM_006718858.3:c.2213-137_2213-136insA	XP_006718921.1:n.2213-137_2213-136insA
NM_001271162.2:c.431-137_431-136insA	NP_001258091.1:n.431-137_431-136insA
NR_073141.3:n.2220-137_2220-136insA
NR_073142.3:n.2103-137_2103-136insA
NR_073143.3:n.1914-137_1914-136insA