Canonical Allele Identifier: CA1995697792

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101128040C= , CM000673.2:g.101128040C=	GRCh38
NC_000011.9:g.100998771C= , CM000673.1:g.100998771C=	GRCh37
NC_000011.8:g.100503981C=	NCBI36
NG_016475.1:g.6774G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.1031G= MANE Select	ENSP00000325120.5:p.Ser344=
ENST00000263463.9:c.1031G=	ENSP00000263463.5:p.Ser344=
ENST00000325455.9:c.1031G=	ENSP00000325120.5:p.Ser344=
ENST00000526300.5:c.1031G=	ENSP00000436803.1:p.Ser344=
ENST00000528960.5:c.1031G=	ENSP00000432914.1:p.Ser344=
ENST00000534013.5:c.-146+1388G=	ENSP00000436561.1:n.-146+1388G=
ENST00000534780.5:c.1031G=	ENSP00000432352.1:p.Ser344=
ENST00000617858.4:c.1031G=	ENSP00000481227.1:p.Ser344=
ENST00000619228.2:c.1031G=	ENSP00000482698.1:p.Ser344=
NM_000926.4:c.1031G= MANE Select	NP_000917.3:p.Ser344=
NM_001202474.3:c.539G=	NP_001189403.1:p.Ser180=
NM_001271161.2:c.539G=	NP_001258090.1:p.Ser180=
NM_001271162.1:c.-146+1388G=	NP_001258091.1:n.-146+1388G=
NR_073141.2:n.1024G=
NR_073142.2:n.1024G=
NR_073143.2:n.1024G=
XM_006718858.2:c.1031G=	XP_006718921.1:p.Ser344=
XM_011542869.1:c.1031G=	XP_011541171.1:p.Ser344=
XR_947831.1:n.2603G=
XM_006718858.3:c.1031G=	XP_006718921.1:p.Ser344=
XM_011542869.2:c.1031G=	XP_011541171.1:p.Ser344=
NM_001271162.2:c.-146+1388G=	NP_001258091.1:n.-146+1388G=
NR_073141.3:n.1038G=
NR_073142.3:n.1038G=
NR_073143.3:n.1038G=