Canonical Allele Identifier: CA382437175

Gene: PGR

Linked Data

• dbSNP Id: rs1565339048
• gnomAD v4: 11-101062686-T-C
• COSMIC: COSM6130639 ; COSM6130640
• MyVariant Identifiers: chr11:g.100933417T>C (hg19) ; chr11:g.101062686T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062686T>C , CM000673.2:g.101062686T>C	GRCh38
NC_000011.9:g.100933417T>C , CM000673.1:g.100933417T>C	GRCh37
NC_000011.8:g.100438627T>C	NCBI36
NG_016475.1:g.72128A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.1973A>G MANE Select	ENSP00000325120.5:p.Gln658Arg
ENST00000263463.9:c.1907-11118A>G	ENSP00000263463.5:n.1907-11118A>G
ENST00000325455.9:c.1973A>G	ENSP00000325120.5:p.Gln658Arg
ENST00000526300.5:c.1907-11118A>G	ENSP00000436803.1:n.1907-11118A>G
ENST00000528960.5:c.1856A>G	ENSP00000432914.1:p.Gln619Arg
ENST00000533207.5:n.1340A>G
ENST00000534013.5:c.191A>G	ENSP00000436561.1:p.Gln64Arg
ENST00000534780.5:c.1973A>G	ENSP00000432352.1:p.Gln658Arg
ENST00000617858.4:c.1907-11118A>G	ENSP00000481227.1:n.1907-11118A>G
ENST00000619228.2:c.1856A>G	ENSP00000482698.1:p.Gln619Arg
ENST00000632634.1:c.395A>G	ENSP00000487607.1:p.Gln132Arg
NM_000926.4:c.1973A>G MANE Select	NP_000917.3:p.Gln658Arg
NM_001202474.3:c.1481A>G	NP_001189403.1:p.Gln494Arg
NM_001271161.2:c.1415-11118A>G	NP_001258090.1:n.1415-11118A>G
NM_001271162.1:c.191A>G	NP_001258091.1:p.Gln64Arg
NR_073141.2:n.1966A>G
NR_073142.2:n.1849A>G
NR_073143.2:n.1900-11118A>G
XM_006718858.2:c.1973A>G	XP_006718921.1:p.Gln658Arg
XR_947831.1:n.3545A>G
XM_006718858.3:c.1973A>G	XP_006718921.1:p.Gln658Arg
NM_001271162.2:c.191A>G	NP_001258091.1:p.Gln64Arg
NR_073141.3:n.1980A>G
NR_073142.3:n.1863A>G
NR_073143.3:n.1914-11118A>G