Canonical Allele Identifier: CA476501664

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922298A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051567A>G , CM000673.2:g.101051567A>G	GRCh38
NC_000011.9:g.100922298A>G , CM000673.1:g.100922298A>G	GRCh37
NC_000011.8:g.100427508A>G	NCBI36
NG_016475.1:g.83247T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2214T>C MANE Select	ENSP00000325120.5:p.Gly738=
ENST00000263463.9:c.1908T>C	ENSP00000263463.5:p.Gly636=
ENST00000325455.9:c.2214T>C	ENSP00000325120.5:p.Gly738=
ENST00000526300.5:c.1908T>C	ENSP00000436803.1:p.Gly636=
ENST00000528960.5:c.2097T>C	ENSP00000432914.1:p.Gly699=
ENST00000533207.5:n.1581T>C
ENST00000534013.5:c.432T>C	ENSP00000436561.1:p.Gly144=
ENST00000534780.5:c.2214T>C	ENSP00000432352.1:p.Gly738=
ENST00000617858.4:c.1908T>C	ENSP00000481227.1:p.Gly636=
ENST00000619228.2:c.2097T>C	ENSP00000482698.1:p.Gly699=
NM_000926.4:c.2214T>C MANE Select	NP_000917.3:p.Gly738=
NM_001202474.3:c.1722T>C	NP_001189403.1:p.Gly574=
NM_001271161.2:c.1416T>C	NP_001258090.1:p.Gly472=
NM_001271162.1:c.432T>C	NP_001258091.1:p.Gly144=
NR_073141.2:n.2207T>C
NR_073142.2:n.2090T>C
NR_073143.2:n.1901T>C
XM_006718858.2:c.2214T>C	XP_006718921.1:p.Gly738=
XR_947831.1:n.3895T>C
XM_006718858.3:c.2214T>C	XP_006718921.1:p.Gly738=
NM_001271162.2:c.432T>C	NP_001258091.1:p.Gly144=
NR_073141.3:n.2221T>C
NR_073142.3:n.2104T>C
NR_073143.3:n.1915T>C