Canonical Allele Identifier: CA1995643477

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101045163T= , CM000673.2:g.101045163T=	GRCh38
NC_000011.9:g.100915894T= , CM000673.1:g.100915894T=	GRCh37
NC_000011.8:g.100421104T=	NCBI36
NG_016475.1:g.89651A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000926.4:c.2489-3061A= MANE Select	NP_000917.3:n.2489-3061A=
ENST00000325455.10:c.2489-3061A= MANE Select	ENSP00000325120.5:n.2489-3061A=
NM_001202474.3:c.1997-3061A=	NP_001189403.1:n.1997-3061A=
NM_001271161.2:c.1691-3061A=	NP_001258090.1:n.1691-3061A=
NM_001271162.1:c.707-3061A=	NP_001258091.1:n.707-3061A=
NM_001271162.2:c.707-3061A=	NP_001258091.1:n.707-3061A=
NR_073141.2:n.2430-3061A=
NR_073141.3:n.2444-3061A=
NR_073142.2:n.2313-3061A=
NR_073142.3:n.2327-3061A=
NR_073143.2:n.2045-3061A=
NR_073143.3:n.2059-3061A=
ENST00000263463.9:c.2183-3061A=	ENSP00000263463.5:n.2183-3061A=
ENST00000325455.9:c.2489-3061A=	ENSP00000325120.5:n.2489-3061A=
ENST00000526300.5:c.2052-3061A=	ENSP00000436803.1:n.2052-3061A=
ENST00000528960.5:c.2320-3061A=	ENSP00000432914.1:n.2320-3061A=
ENST00000530764.1:n.179-3061A=
ENST00000533207.5:n.1856-3061A=
ENST00000534013.5:c.707-3061A=	ENSP00000436561.1:n.707-3061A=
ENST00000534780.5:c.2437-3061A=	ENSP00000432352.1:n.2437-3061A=
XM_006718858.2:c.2358-3061A=	XP_006718921.1:n.2358-3061A=
XM_006718858.3:c.2358-3061A=	XP_006718921.1:n.2358-3061A=