Canonical Allele Identifier: CA382436202

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922224A>G (hg19) ; chr11:g.101051493A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051493A>G , CM000673.2:g.101051493A>G	GRCh38
NC_000011.9:g.100922224A>G , CM000673.1:g.100922224A>G	GRCh37
NC_000011.8:g.100427434A>G	NCBI36
NG_016475.1:g.83321T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2288T>C MANE Select	ENSP00000325120.5:p.Leu763Pro
ENST00000263463.9:c.1982T>C	ENSP00000263463.5:p.Leu661Pro
ENST00000325455.9:c.2288T>C	ENSP00000325120.5:p.Leu763Pro
ENST00000526300.5:c.1982T>C	ENSP00000436803.1:p.Leu661Pro
ENST00000528960.5:c.2171T>C	ENSP00000432914.1:p.Leu724Pro
ENST00000533207.5:n.1655T>C
ENST00000534013.5:c.506T>C	ENSP00000436561.1:p.Leu169Pro
ENST00000534780.5:c.2288T>C	ENSP00000432352.1:p.Leu763Pro
ENST00000617858.4:c.1982T>C	ENSP00000481227.1:p.Leu661Pro
ENST00000619228.2:c.2171T>C	ENSP00000482698.1:p.Leu724Pro
NM_000926.4:c.2288T>C MANE Select	NP_000917.3:p.Leu763Pro
NM_001202474.3:c.1796T>C	NP_001189403.1:p.Leu599Pro
NM_001271161.2:c.1490T>C	NP_001258090.1:p.Leu497Pro
NM_001271162.1:c.506T>C	NP_001258091.1:p.Leu169Pro
NR_073141.2:n.2281T>C
NR_073142.2:n.2164T>C
NR_073143.2:n.1975T>C
XM_006718858.2:c.2288T>C	XP_006718921.1:p.Leu763Pro
XM_006718858.3:c.2288T>C	XP_006718921.1:p.Leu763Pro
NM_001271162.2:c.506T>C	NP_001258091.1:p.Leu169Pro
NR_073141.3:n.2295T>C
NR_073142.3:n.2178T>C
NR_073143.3:n.1989T>C