Canonical Allele Identifier: CA601426498

Gene: PGR

Linked Data

• dbSNP Id: rs1320850860
• gnomAD v2: 11-100921608-G-A
• gnomAD v3: 11-101050877-G-A
• gnomAD v4: 11-101050877-G-A
• MyVariant Identifiers: chr11:g.100921608G>A (hg19) ; chr11:g.101050877G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050877G>A , CM000673.2:g.101050877G>A	GRCh38
NC_000011.9:g.100921608G>A , CM000673.1:g.100921608G>A	GRCh37
NC_000011.8:g.100426818G>A	NCBI36
NG_016475.1:g.83937C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+547C>T MANE Select	ENSP00000325120.5:n.2357+547C>T
ENST00000263463.9:c.2051+547C>T	ENSP00000263463.5:n.2051+547C>T
ENST00000325455.9:c.2357+547C>T	ENSP00000325120.5:n.2357+547C>T
ENST00000526300.5:c.2051+547C>T	ENSP00000436803.1:n.2051+547C>T
ENST00000528960.5:c.2240+547C>T	ENSP00000432914.1:n.2240+547C>T
ENST00000530764.1:n.47+547C>T
ENST00000533207.5:n.1724+547C>T
ENST00000534013.5:c.575+547C>T	ENSP00000436561.1:n.575+547C>T
ENST00000534780.5:c.2357+547C>T	ENSP00000432352.1:n.2357+547C>T
ENST00000617858.4:c.2052+72C>T	ENSP00000481227.1:n.2052+72C>T
ENST00000619228.2:c.2240+547C>T	ENSP00000482698.1:n.2240+547C>T
NM_000926.4:c.2357+547C>T MANE Select	NP_000917.3:n.2357+547C>T
NM_001202474.3:c.1865+547C>T	NP_001189403.1:n.1865+547C>T
NM_001271161.2:c.1559+547C>T	NP_001258090.1:n.1559+547C>T
NM_001271162.1:c.575+547C>T	NP_001258091.1:n.575+547C>T
NR_073141.2:n.2350+547C>T
NR_073142.2:n.2233+547C>T
NR_073143.2:n.2044+547C>T
XM_006718858.2:c.2357+547C>T	XP_006718921.1:n.2357+547C>T
XM_006718858.3:c.2357+547C>T	XP_006718921.1:n.2357+547C>T
NM_001271162.2:c.575+547C>T	NP_001258091.1:n.575+547C>T
NR_073141.3:n.2364+547C>T
NR_073142.3:n.2247+547C>T
NR_073143.3:n.2058+547C>T