Canonical Allele Identifier: CA2615679990

Gene: PGR

Linked Data

• gnomAD v4: 11-101051694-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051697_101051698del , CM000673.2:g.101051697_101051698del	GRCh38
NC_000011.9:g.100922428_100922429del , CM000673.1:g.100922428_100922429del	GRCh37
NC_000011.8:g.100427638_100427639del	NCBI36
NG_016475.1:g.83118_83119del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2213-128_2213-127del MANE Select	ENSP00000325120.5:n.2213-128_2213-127del
ENST00000263463.9:c.1907-128_1907-127del	ENSP00000263463.5:n.1907-128_1907-127del
ENST00000325455.9:c.2213-128_2213-127del	ENSP00000325120.5:n.2213-128_2213-127del
ENST00000526300.5:c.1907-128_1907-127del	ENSP00000436803.1:n.1907-128_1907-127del
ENST00000528960.5:c.2096-128_2096-127del	ENSP00000432914.1:n.2096-128_2096-127del
ENST00000533207.5:n.1580-128_1580-127del
ENST00000534013.5:c.431-128_431-127del	ENSP00000436561.1:n.431-128_431-127del
ENST00000534780.5:c.2213-128_2213-127del	ENSP00000432352.1:n.2213-128_2213-127del
ENST00000617858.4:c.1907-128_1907-127del	ENSP00000481227.1:n.1907-128_1907-127del
ENST00000619228.2:c.2096-128_2096-127del	ENSP00000482698.1:n.2096-128_2096-127del
NM_000926.4:c.2213-128_2213-127del MANE Select	NP_000917.3:n.2213-128_2213-127del
NM_001202474.3:c.1721-128_1721-127del	NP_001189403.1:n.1721-128_1721-127del
NM_001271161.2:c.1415-128_1415-127del	NP_001258090.1:n.1415-128_1415-127del
NM_001271162.1:c.431-128_431-127del	NP_001258091.1:n.431-128_431-127del
NR_073141.2:n.2206-128_2206-127del
NR_073142.2:n.2089-128_2089-127del
NR_073143.2:n.1900-128_1900-127del
XM_006718858.2:c.2213-128_2213-127del	XP_006718921.1:n.2213-128_2213-127del
XR_947831.1:n.3894-128_3894-127del
XM_006718858.3:c.2213-128_2213-127del	XP_006718921.1:n.2213-128_2213-127del
NM_001271162.2:c.431-128_431-127del	NP_001258091.1:n.431-128_431-127del
NR_073141.3:n.2220-128_2220-127del
NR_073142.3:n.2103-128_2103-127del
NR_073143.3:n.1914-128_1914-127del