Canonical Allele Identifier: CA3185972797

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062508A= , CM000673.2:g.101062508A=	GRCh38
NC_000011.9:g.100933239A= , CM000673.1:g.100933239A=	GRCh37
NC_000011.8:g.100438449A=	NCBI36
NG_016475.1:g.72306T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000926.4:c.2151T= MANE Select	NP_000917.3:p.Ser717=
ENST00000325455.10:c.2151T= MANE Select	ENSP00000325120.5:p.Ser717=
NM_001202474.3:c.1659T=	NP_001189403.1:p.Ser553=
NM_001271161.2:c.1415-10940T=	NP_001258090.1:n.1415-10940T=
NM_001271162.1:c.369T=	NP_001258091.1:p.Ser123=
NM_001271162.2:c.369T=	NP_001258091.1:p.Ser123=
NR_073141.2:n.2144T=
NR_073141.3:n.2158T=
NR_073142.2:n.2027T=
NR_073142.3:n.2041T=
NR_073143.2:n.1900-10940T=
NR_073143.3:n.1914-10940T=
ENST00000263463.9:c.1907-10940T=	ENSP00000263463.5:n.1907-10940T=
ENST00000325455.9:c.2151T=	ENSP00000325120.5:p.Ser717=
ENST00000526300.5:c.1907-10940T=	ENSP00000436803.1:n.1907-10940T=
ENST00000528960.5:c.2034T=	ENSP00000432914.1:p.Ser678=
ENST00000533207.5:n.1518T=
ENST00000534013.5:c.369T=	ENSP00000436561.1:p.Ser123=
ENST00000534780.5:c.2151T=	ENSP00000432352.1:p.Ser717=
ENST00000617858.4:c.1907-10940T=	ENSP00000481227.1:n.1907-10940T=
ENST00000619228.2:c.2034T=	ENSP00000482698.1:p.Ser678=
XM_006718858.2:c.2151T=	XP_006718921.1:p.Ser717=
XM_006718858.3:c.2151T=	XP_006718921.1:p.Ser717=
XR_947831.1:n.3723T=