Canonical Allele Identifier: CA382436323

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922274G>C (hg19) ; chr11:g.101051543G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051543G>C , CM000673.2:g.101051543G>C	GRCh38
NC_000011.9:g.100922274G>C , CM000673.1:g.100922274G>C	GRCh37
NC_000011.8:g.100427484G>C	NCBI36
NG_016475.1:g.83271C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2238C>G MANE Select	ENSP00000325120.5:p.Asp746Glu
ENST00000263463.9:c.1932C>G	ENSP00000263463.5:p.Asp644Glu
ENST00000325455.9:c.2238C>G	ENSP00000325120.5:p.Asp746Glu
ENST00000526300.5:c.1932C>G	ENSP00000436803.1:p.Asp644Glu
ENST00000528960.5:c.2121C>G	ENSP00000432914.1:p.Asp707Glu
ENST00000533207.5:n.1605C>G
ENST00000534013.5:c.456C>G	ENSP00000436561.1:p.Asp152Glu
ENST00000534780.5:c.2238C>G	ENSP00000432352.1:p.Asp746Glu
ENST00000617858.4:c.1932C>G	ENSP00000481227.1:p.Asp644Glu
ENST00000619228.2:c.2121C>G	ENSP00000482698.1:p.Asp707Glu
NM_000926.4:c.2238C>G MANE Select	NP_000917.3:p.Asp746Glu
NM_001202474.3:c.1746C>G	NP_001189403.1:p.Asp582Glu
NM_001271161.2:c.1440C>G	NP_001258090.1:p.Asp480Glu
NM_001271162.1:c.456C>G	NP_001258091.1:p.Asp152Glu
NR_073141.2:n.2231C>G
NR_073142.2:n.2114C>G
NR_073143.2:n.1925C>G
XM_006718858.2:c.2238C>G	XP_006718921.1:p.Asp746Glu
XR_947831.1:n.3919C>G
XM_006718858.3:c.2238C>G	XP_006718921.1:p.Asp746Glu
NM_001271162.2:c.456C>G	NP_001258091.1:p.Asp152Glu
NR_073141.3:n.2245C>G
NR_073142.3:n.2128C>G
NR_073143.3:n.1939C>G