Canonical Allele Identifier: CA1995654429

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051444T= , CM000673.2:g.101051444T=	GRCh38
NC_000011.9:g.100922175T= , CM000673.1:g.100922175T=	GRCh37
NC_000011.8:g.100427385T=	NCBI36
NG_016475.1:g.83370A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2337A= MANE Select	ENSP00000325120.5:p.Ala779=
ENST00000263463.9:c.2031A=	ENSP00000263463.5:p.Ala677=
ENST00000325455.9:c.2337A=	ENSP00000325120.5:p.Ala779=
ENST00000526300.5:c.2031A=	ENSP00000436803.1:p.Ala677=
ENST00000528960.5:c.2220A=	ENSP00000432914.1:p.Ala740=
ENST00000530764.1:n.27A=
ENST00000533207.5:n.1704A=
ENST00000534013.5:c.555A=	ENSP00000436561.1:p.Ala185=
ENST00000534780.5:c.2337A=	ENSP00000432352.1:p.Ala779=
ENST00000617858.4:c.2031A=	ENSP00000481227.1:p.Ala677=
ENST00000619228.2:c.2220A=	ENSP00000482698.1:p.Ala740=
NM_000926.4:c.2337A= MANE Select	NP_000917.3:p.Ala779=
NM_001202474.3:c.1845A=	NP_001189403.1:p.Ala615=
NM_001271161.2:c.1539A=	NP_001258090.1:p.Ala513=
NM_001271162.1:c.555A=	NP_001258091.1:p.Ala185=
NR_073141.2:n.2330A=
NR_073142.2:n.2213A=
NR_073143.2:n.2024A=
XM_006718858.2:c.2337A=	XP_006718921.1:p.Ala779=
XM_006718858.3:c.2337A=	XP_006718921.1:p.Ala779=
NM_001271162.2:c.555A=	NP_001258091.1:p.Ala185=
NR_073141.3:n.2344A=
NR_073142.3:n.2227A=
NR_073143.3:n.2038A=