Canonical Allele Identifier: CA1995653642

Gene: PGR

Linked Data

• dbSNP Id: rs1860066709

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050959_101050960insATA , CM000673.2:g.101050959_101050960insATA	GRCh38
NC_000011.9:g.100921690_100921691insATA , CM000673.1:g.100921690_100921691insATA	GRCh37
NC_000011.8:g.100426900_100426901insATA	NCBI36
NG_016475.1:g.83854_83855insTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+464_2357+465insTAT MANE Select	ENSP00000325120.5:n.2357+464_2357+465insTAT
ENST00000263463.9:c.2051+464_2051+465insTAT	ENSP00000263463.5:n.2051+464_2051+465insTAT
ENST00000325455.9:c.2357+464_2357+465insTAT	ENSP00000325120.5:n.2357+464_2357+465insTAT
ENST00000526300.5:c.2051+464_2051+465insTAT	ENSP00000436803.1:n.2051+464_2051+465insTAT
ENST00000528960.5:c.2240+464_2240+465insTAT	ENSP00000432914.1:n.2240+464_2240+465insTAT
ENST00000530764.1:n.47+464_47+465insTAT
ENST00000533207.5:n.1724+464_1724+465insTAT
ENST00000534013.5:c.575+464_575+465insTAT	ENSP00000436561.1:n.575+464_575+465insTAT
ENST00000534780.5:c.2357+464_2357+465insTAT	ENSP00000432352.1:n.2357+464_2357+465insTAT
ENST00000617858.4:c.2052-11_2052-10insTAT	ENSP00000481227.1:n.2052-11_2052-10insTAT
ENST00000619228.2:c.2240+464_2240+465insTAT	ENSP00000482698.1:n.2240+464_2240+465insTAT
NM_000926.4:c.2357+464_2357+465insTAT MANE Select	NP_000917.3:n.2357+464_2357+465insTAT
NM_001202474.3:c.1865+464_1865+465insTAT	NP_001189403.1:n.1865+464_1865+465insTAT
NM_001271161.2:c.1559+464_1559+465insTAT	NP_001258090.1:n.1559+464_1559+465insTAT
NM_001271162.1:c.575+464_575+465insTAT	NP_001258091.1:n.575+464_575+465insTAT
NR_073141.2:n.2350+464_2350+465insTAT
NR_073142.2:n.2233+464_2233+465insTAT
NR_073143.2:n.2044+464_2044+465insTAT
XM_006718858.2:c.2357+464_2357+465insTAT	XP_006718921.1:n.2357+464_2357+465insTAT
XM_006718858.3:c.2357+464_2357+465insTAT	XP_006718921.1:n.2357+464_2357+465insTAT
NM_001271162.2:c.575+464_575+465insTAT	NP_001258091.1:n.575+464_575+465insTAT
NR_073141.3:n.2364+464_2364+465insTAT
NR_073142.3:n.2247+464_2247+465insTAT
NR_073143.3:n.2058+464_2058+465insTAT