Canonical Allele Identifier: CA382436248

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922243T>G (hg19) ; chr11:g.101051512T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051512T>G , CM000673.2:g.101051512T>G	GRCh38
NC_000011.9:g.100922243T>G , CM000673.1:g.100922243T>G	GRCh37
NC_000011.8:g.100427453T>G	NCBI36
NG_016475.1:g.83302A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2269A>C MANE Select	ENSP00000325120.5:p.Ser757Arg
ENST00000263463.9:c.1963A>C	ENSP00000263463.5:p.Ser655Arg
ENST00000325455.9:c.2269A>C	ENSP00000325120.5:p.Ser757Arg
ENST00000526300.5:c.1963A>C	ENSP00000436803.1:p.Ser655Arg
ENST00000528960.5:c.2152A>C	ENSP00000432914.1:p.Ser718Arg
ENST00000533207.5:n.1636A>C
ENST00000534013.5:c.487A>C	ENSP00000436561.1:p.Ser163Arg
ENST00000534780.5:c.2269A>C	ENSP00000432352.1:p.Ser757Arg
ENST00000617858.4:c.1963A>C	ENSP00000481227.1:p.Ser655Arg
ENST00000619228.2:c.2152A>C	ENSP00000482698.1:p.Ser718Arg
NM_000926.4:c.2269A>C MANE Select	NP_000917.3:p.Ser757Arg
NM_001202474.3:c.1777A>C	NP_001189403.1:p.Ser593Arg
NM_001271161.2:c.1471A>C	NP_001258090.1:p.Ser491Arg
NM_001271162.1:c.487A>C	NP_001258091.1:p.Ser163Arg
NR_073141.2:n.2262A>C
NR_073142.2:n.2145A>C
NR_073143.2:n.1956A>C
XM_006718858.2:c.2269A>C	XP_006718921.1:p.Ser757Arg
XR_947831.1:n.3950A>C
XM_006718858.3:c.2269A>C	XP_006718921.1:p.Ser757Arg
NM_001271162.2:c.487A>C	NP_001258091.1:p.Ser163Arg
NR_073141.3:n.2276A>C
NR_073142.3:n.2159A>C
NR_073143.3:n.1970A>C