Canonical Allele Identifier: CA1995653598

Gene: PGR

Linked Data

• dbSNP Id: rs1860065846

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050954_101050955insTTATATTTATATACTG , CM000673.2:g.101050954_101050955insTTATATTTATATACTG	GRCh38
NC_000011.9:g.100921685_100921686insTTATATTTATATACTG , CM000673.1:g.100921685_100921686insTTATATTTATATACTG	GRCh37
NC_000011.8:g.100426895_100426896insTTATATTTATATACTG	NCBI36
NG_016475.1:g.83859_83860insCAGTATATAAATATAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+469_2357+470insCAGTATATAAATATAA MANE Select	ENSP00000325120.5:n.2357+469_2357+470insCAGTATATAAATATAA
ENST00000263463.9:c.2051+469_2051+470insCAGTATATAAATATAA	ENSP00000263463.5:n.2051+469_2051+470insCAGTATATAAATATAA
ENST00000325455.9:c.2357+469_2357+470insCAGTATATAAATATAA	ENSP00000325120.5:n.2357+469_2357+470insCAGTATATAAATATAA
ENST00000526300.5:c.2051+469_2051+470insCAGTATATAAATATAA	ENSP00000436803.1:n.2051+469_2051+470insCAGTATATAAATATAA
ENST00000528960.5:c.2240+469_2240+470insCAGTATATAAATATAA	ENSP00000432914.1:n.2240+469_2240+470insCAGTATATAAATATAA
ENST00000530764.1:n.47+469_47+470insCAGTATATAAATATAA
ENST00000533207.5:n.1724+469_1724+470insCAGTATATAAATATAA
ENST00000534013.5:c.575+469_575+470insCAGTATATAAATATAA	ENSP00000436561.1:n.575+469_575+470insCAGTATATAAATATAA
ENST00000534780.5:c.2357+469_2357+470insCAGTATATAAATATAA	ENSP00000432352.1:n.2357+469_2357+470insCAGTATATAAATATAA
ENST00000617858.4:c.2052-6_2052-5insCAGTATATAAATATAA	ENSP00000481227.1:n.2052-6_2052-5insCAGTATATAAATATAA
ENST00000619228.2:c.2240+469_2240+470insCAGTATATAAATATAA	ENSP00000482698.1:n.2240+469_2240+470insCAGTATATAAATATAA
NM_000926.4:c.2357+469_2357+470insCAGTATATAAATATAA MANE Select	NP_000917.3:n.2357+469_2357+470insCAGTATATAAATATAA
NM_001202474.3:c.1865+469_1865+470insCAGTATATAAATATAA	NP_001189403.1:n.1865+469_1865+470insCAGTATATAAATATAA
NM_001271161.2:c.1559+469_1559+470insCAGTATATAAATATAA	NP_001258090.1:n.1559+469_1559+470insCAGTATATAAATATAA
NM_001271162.1:c.575+469_575+470insCAGTATATAAATATAA	NP_001258091.1:n.575+469_575+470insCAGTATATAAATATAA
NR_073141.2:n.2350+469_2350+470insCAGTATATAAATATAA
NR_073142.2:n.2233+469_2233+470insCAGTATATAAATATAA
NR_073143.2:n.2044+469_2044+470insCAGTATATAAATATAA
XM_006718858.2:c.2357+469_2357+470insCAGTATATAAATATAA	XP_006718921.1:n.2357+469_2357+470insCAGTATATAAATATAA
XM_006718858.3:c.2357+469_2357+470insCAGTATATAAATATAA	XP_006718921.1:n.2357+469_2357+470insCAGTATATAAATATAA
NM_001271162.2:c.575+469_575+470insCAGTATATAAATATAA	NP_001258091.1:n.575+469_575+470insCAGTATATAAATATAA
NR_073141.3:n.2364+469_2364+470insCAGTATATAAATATAA
NR_073142.3:n.2247+469_2247+470insCAGTATATAAATATAA
NR_073143.3:n.2058+469_2058+470insCAGTATATAAATATAA