Canonical Allele Identifier: CA1995653995

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062592G= , CM000673.2:g.101062592G=	GRCh38
NC_000011.9:g.100933323G= , CM000673.1:g.100933323G=	GRCh37
NC_000011.8:g.100438533G=	NCBI36
NG_016475.1:g.72222C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2067C= MANE Select	ENSP00000325120.5:p.Asn689=
ENST00000263463.9:c.1907-11024C=	ENSP00000263463.5:n.1907-11024C=
ENST00000325455.9:c.2067C=	ENSP00000325120.5:p.Asn689=
ENST00000526300.5:c.1907-11024C=	ENSP00000436803.1:n.1907-11024C=
ENST00000528960.5:c.1950C=	ENSP00000432914.1:p.Asn650=
ENST00000533207.5:n.1434C=
ENST00000534013.5:c.285C=	ENSP00000436561.1:p.Asn95=
ENST00000534780.5:c.2067C=	ENSP00000432352.1:p.Asn689=
ENST00000617858.4:c.1907-11024C=	ENSP00000481227.1:n.1907-11024C=
ENST00000619228.2:c.1950C=	ENSP00000482698.1:p.Asn650=
ENST00000632634.1:c.489C=	ENSP00000487607.1:p.Asn163=
NM_000926.4:c.2067C= MANE Select	NP_000917.3:p.Asn689=
NM_001202474.3:c.1575C=	NP_001189403.1:p.Asn525=
NM_001271161.2:c.1415-11024C=	NP_001258090.1:n.1415-11024C=
NM_001271162.1:c.285C=	NP_001258091.1:p.Asn95=
NR_073141.2:n.2060C=
NR_073142.2:n.1943C=
NR_073143.2:n.1900-11024C=
XM_006718858.2:c.2067C=	XP_006718921.1:p.Asn689=
XR_947831.1:n.3639C=
XM_006718858.3:c.2067C=	XP_006718921.1:p.Asn689=
NM_001271162.2:c.285C=	NP_001258091.1:p.Asn95=
NR_073141.3:n.2074C=
NR_073142.3:n.1957C=
NR_073143.3:n.1914-11024C=