Canonical Allele Identifier: CA476501652

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922289G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051558G>A , CM000673.2:g.101051558G>A	GRCh38
NC_000011.9:g.100922289G>A , CM000673.1:g.100922289G>A	GRCh37
NC_000011.8:g.100427499G>A	NCBI36
NG_016475.1:g.83256C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2223C>T MANE Select	ENSP00000325120.5:p.Asn741=
ENST00000263463.9:c.1917C>T	ENSP00000263463.5:p.Asn639=
ENST00000325455.9:c.2223C>T	ENSP00000325120.5:p.Asn741=
ENST00000526300.5:c.1917C>T	ENSP00000436803.1:p.Asn639=
ENST00000528960.5:c.2106C>T	ENSP00000432914.1:p.Asn702=
ENST00000533207.5:n.1590C>T
ENST00000534013.5:c.441C>T	ENSP00000436561.1:p.Asn147=
ENST00000534780.5:c.2223C>T	ENSP00000432352.1:p.Asn741=
ENST00000617858.4:c.1917C>T	ENSP00000481227.1:p.Asn639=
ENST00000619228.2:c.2106C>T	ENSP00000482698.1:p.Asn702=
NM_000926.4:c.2223C>T MANE Select	NP_000917.3:p.Asn741=
NM_001202474.3:c.1731C>T	NP_001189403.1:p.Asn577=
NM_001271161.2:c.1425C>T	NP_001258090.1:p.Asn475=
NM_001271162.1:c.441C>T	NP_001258091.1:p.Asn147=
NR_073141.2:n.2216C>T
NR_073142.2:n.2099C>T
NR_073143.2:n.1910C>T
XM_006718858.2:c.2223C>T	XP_006718921.1:p.Asn741=
XR_947831.1:n.3904C>T
XM_006718858.3:c.2223C>T	XP_006718921.1:p.Asn741=
NM_001271162.2:c.441C>T	NP_001258091.1:p.Asn147=
NR_073141.3:n.2230C>T
NR_073142.3:n.2113C>T
NR_073143.3:n.1924C>T