Canonical Allele Identifier: CA2615679897

Gene: PGR

Linked Data

• gnomAD v4: 11-101051419-CTTACTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051422_101051428del , CM000673.2:g.101051422_101051428del	GRCh38
NC_000011.9:g.100922153_100922159del , CM000673.1:g.100922153_100922159del	GRCh37
NC_000011.8:g.100427363_100427369del	NCBI36
NG_016475.1:g.83388_83394del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.2355_2357+4del
ENST00000263463.9:c.2049_2051+4del
ENST00000325455.9:c.2355_2357+4del
ENST00000526300.5:c.2049_2051+4del
ENST00000528960.5:c.2238_2240+4del
ENST00000530764.1:n.45_47+4del
ENST00000533207.5:n.1722_1724+4del
ENST00000534013.5:c.573_575+4del
ENST00000534780.5:c.2355_2357+4del
ENST00000617858.4:c.2049_2051+4del
ENST00000619228.2:c.2238_2240+4del
NM_000926.4:c.2355_2357+4del
NM_001202474.3:c.1863_1865+4del
NM_001271161.2:c.1557_1559+4del
NM_001271162.1:c.573_575+4del
NR_073141.2:n.2348_2350+4del
NR_073142.2:n.2231_2233+4del
NR_073143.2:n.2042_2044+4del
XM_006718858.2:c.2355_2357+4del
XM_006718858.3:c.2355_2357+4del
NM_001271162.2:c.573_575+4del
NR_073141.3:n.2362_2364+4del
NR_073142.3:n.2245_2247+4del
NR_073143.3:n.2056_2058+4del