Canonical Allele Identifier: CA1995640368

Gene: PGR

Linked Data

• dbSNP Id: rs1860095522

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051730_101051731del , CM000673.2:g.101051730_101051731del	GRCh38
NC_000011.9:g.100922461_100922462del , CM000673.1:g.100922461_100922462del	GRCh37
NC_000011.8:g.100427671_100427672del	NCBI36
NG_016475.1:g.83084_83085del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2213-162_2213-161del MANE Select	ENSP00000325120.5:n.2213-162_2213-161del
ENST00000263463.9:c.1907-162_1907-161del	ENSP00000263463.5:n.1907-162_1907-161del
ENST00000325455.9:c.2213-162_2213-161del	ENSP00000325120.5:n.2213-162_2213-161del
ENST00000526300.5:c.1907-162_1907-161del	ENSP00000436803.1:n.1907-162_1907-161del
ENST00000528960.5:c.2096-162_2096-161del	ENSP00000432914.1:n.2096-162_2096-161del
ENST00000533207.5:n.1580-162_1580-161del
ENST00000534013.5:c.431-162_431-161del	ENSP00000436561.1:n.431-162_431-161del
ENST00000534780.5:c.2213-162_2213-161del	ENSP00000432352.1:n.2213-162_2213-161del
ENST00000617858.4:c.1907-162_1907-161del	ENSP00000481227.1:n.1907-162_1907-161del
ENST00000619228.2:c.2096-162_2096-161del	ENSP00000482698.1:n.2096-162_2096-161del
NM_000926.4:c.2213-162_2213-161del MANE Select	NP_000917.3:n.2213-162_2213-161del
NM_001202474.3:c.1721-162_1721-161del	NP_001189403.1:n.1721-162_1721-161del
NM_001271161.2:c.1415-162_1415-161del	NP_001258090.1:n.1415-162_1415-161del
NM_001271162.1:c.431-162_431-161del	NP_001258091.1:n.431-162_431-161del
NR_073141.2:n.2206-162_2206-161del
NR_073142.2:n.2089-162_2089-161del
NR_073143.2:n.1900-162_1900-161del
XM_006718858.2:c.2213-162_2213-161del	XP_006718921.1:n.2213-162_2213-161del
XR_947831.1:n.3894-162_3894-161del
XM_006718858.3:c.2213-162_2213-161del	XP_006718921.1:n.2213-162_2213-161del
NM_001271162.2:c.431-162_431-161del	NP_001258091.1:n.431-162_431-161del
NR_073141.3:n.2220-162_2220-161del
NR_073142.3:n.2103-162_2103-161del
NR_073143.3:n.1914-162_1914-161del