Canonical Allele Identifier: CA1995640395

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051764T= , CM000673.2:g.101051764T=	GRCh38
NC_000011.9:g.100922495T= , CM000673.1:g.100922495T=	GRCh37
NC_000011.8:g.100427705T=	NCBI36
NG_016475.1:g.83050A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2213-196A= MANE Select	ENSP00000325120.5:n.2213-196A=
ENST00000263463.9:c.1907-196A=	ENSP00000263463.5:n.1907-196A=
ENST00000325455.9:c.2213-196A=	ENSP00000325120.5:n.2213-196A=
ENST00000526300.5:c.1907-196A=	ENSP00000436803.1:n.1907-196A=
ENST00000528960.5:c.2096-196A=	ENSP00000432914.1:n.2096-196A=
ENST00000533207.5:n.1580-196A=
ENST00000534013.5:c.431-196A=	ENSP00000436561.1:n.431-196A=
ENST00000534780.5:c.2213-196A=	ENSP00000432352.1:n.2213-196A=
ENST00000617858.4:c.1907-196A=	ENSP00000481227.1:n.1907-196A=
ENST00000619228.2:c.2096-196A=	ENSP00000482698.1:n.2096-196A=
NM_000926.4:c.2213-196A= MANE Select	NP_000917.3:n.2213-196A=
NM_001202474.3:c.1721-196A=	NP_001189403.1:n.1721-196A=
NM_001271161.2:c.1415-196A=	NP_001258090.1:n.1415-196A=
NM_001271162.1:c.431-196A=	NP_001258091.1:n.431-196A=
NR_073141.2:n.2206-196A=
NR_073142.2:n.2089-196A=
NR_073143.2:n.1900-196A=
XM_006718858.2:c.2213-196A=	XP_006718921.1:n.2213-196A=
XR_947831.1:n.3894-196A=
XM_006718858.3:c.2213-196A=	XP_006718921.1:n.2213-196A=
NM_001271162.2:c.431-196A=	NP_001258091.1:n.431-196A=
NR_073141.3:n.2220-196A=
NR_073142.3:n.2103-196A=
NR_073143.3:n.1914-196A=