Canonical Allele Identifier: CA382436211

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922228C>G (hg19) ; chr11:g.101051497C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051497C>G , CM000673.2:g.101051497C>G	GRCh38
NC_000011.9:g.100922228C>G , CM000673.1:g.100922228C>G	GRCh37
NC_000011.8:g.100427438C>G	NCBI36
NG_016475.1:g.83317G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2284G>C MANE Select	ENSP00000325120.5:p.Gly762Arg
ENST00000263463.9:c.1978G>C	ENSP00000263463.5:p.Gly660Arg
ENST00000325455.9:c.2284G>C	ENSP00000325120.5:p.Gly762Arg
ENST00000526300.5:c.1978G>C	ENSP00000436803.1:p.Gly660Arg
ENST00000528960.5:c.2167G>C	ENSP00000432914.1:p.Gly723Arg
ENST00000533207.5:n.1651G>C
ENST00000534013.5:c.502G>C	ENSP00000436561.1:p.Gly168Arg
ENST00000534780.5:c.2284G>C	ENSP00000432352.1:p.Gly762Arg
ENST00000617858.4:c.1978G>C	ENSP00000481227.1:p.Gly660Arg
ENST00000619228.2:c.2167G>C	ENSP00000482698.1:p.Gly723Arg
NM_000926.4:c.2284G>C MANE Select	NP_000917.3:p.Gly762Arg
NM_001202474.3:c.1792G>C	NP_001189403.1:p.Gly598Arg
NM_001271161.2:c.1486G>C	NP_001258090.1:p.Gly496Arg
NM_001271162.1:c.502G>C	NP_001258091.1:p.Gly168Arg
NR_073141.2:n.2277G>C
NR_073142.2:n.2160G>C
NR_073143.2:n.1971G>C
XM_006718858.2:c.2284G>C	XP_006718921.1:p.Gly762Arg
XR_947831.1:n.3965G>C
XM_006718858.3:c.2284G>C	XP_006718921.1:p.Gly762Arg
NM_001271162.2:c.502G>C	NP_001258091.1:p.Gly168Arg
NR_073141.3:n.2291G>C
NR_073142.3:n.2174G>C
NR_073143.3:n.1985G>C