Canonical Allele Identifier: CA1995653684

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101050985A= , CM000673.2:g.101050985A=	GRCh38
NC_000011.9:g.100921716A= , CM000673.1:g.100921716A=	GRCh37
NC_000011.8:g.100426926A=	NCBI36
NG_016475.1:g.83829T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2357+439T= MANE Select	ENSP00000325120.5:n.2357+439T=
ENST00000263463.9:c.2051+439T=	ENSP00000263463.5:n.2051+439T=
ENST00000325455.9:c.2357+439T=	ENSP00000325120.5:n.2357+439T=
ENST00000526300.5:c.2051+439T=	ENSP00000436803.1:n.2051+439T=
ENST00000528960.5:c.2240+439T=	ENSP00000432914.1:n.2240+439T=
ENST00000530764.1:n.47+439T=
ENST00000533207.5:n.1724+439T=
ENST00000534013.5:c.575+439T=	ENSP00000436561.1:n.575+439T=
ENST00000534780.5:c.2357+439T=	ENSP00000432352.1:n.2357+439T=
ENST00000617858.4:c.2052-36T=	ENSP00000481227.1:n.2052-36T=
ENST00000619228.2:c.2240+439T=	ENSP00000482698.1:n.2240+439T=
NM_000926.4:c.2357+439T= MANE Select	NP_000917.3:n.2357+439T=
NM_001202474.3:c.1865+439T=	NP_001189403.1:n.1865+439T=
NM_001271161.2:c.1559+439T=	NP_001258090.1:n.1559+439T=
NM_001271162.1:c.575+439T=	NP_001258091.1:n.575+439T=
NR_073141.2:n.2350+439T=
NR_073142.2:n.2233+439T=
NR_073143.2:n.2044+439T=
XM_006718858.2:c.2357+439T=	XP_006718921.1:n.2357+439T=
XM_006718858.3:c.2357+439T=	XP_006718921.1:n.2357+439T=
NM_001271162.2:c.575+439T=	NP_001258091.1:n.575+439T=
NR_073141.3:n.2364+439T=
NR_073142.3:n.2247+439T=
NR_073143.3:n.2058+439T=