Canonical Allele Identifier: CA1995658507

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101103335A= , CM000673.2:g.101103335A=	GRCh38
NC_000011.9:g.100974066A= , CM000673.1:g.100974066A=	GRCh37
NC_000011.8:g.100479276A=	NCBI36
NG_016475.1:g.31479T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.1790-11459T= MANE Select	ENSP00000325120.5:n.1790-11459T=
ENST00000263463.9:c.1790-11459T=	ENSP00000263463.5:n.1790-11459T=
ENST00000325455.9:c.1790-11459T=	ENSP00000325120.5:n.1790-11459T=
ENST00000526300.5:c.1790-11459T=	ENSP00000436803.1:n.1790-11459T=
ENST00000528960.5:c.1789+22672T=	ENSP00000432914.1:n.1789+22672T=
ENST00000534013.5:c.8-11459T=	ENSP00000436561.1:n.8-11459T=
ENST00000534780.5:c.1790-11459T=	ENSP00000432352.1:n.1790-11459T=
ENST00000617858.4:c.1790-11459T=	ENSP00000481227.1:n.1790-11459T=
ENST00000619228.2:c.1789+22672T=	ENSP00000482698.1:n.1789+22672T=
ENST00000632634.1:c.212-11459T=	ENSP00000487607.1:n.212-11459T=
NM_000926.4:c.1790-11459T= MANE Select	NP_000917.3:n.1790-11459T=
NM_001202474.3:c.1298-11459T=	NP_001189403.1:n.1298-11459T=
NM_001271161.2:c.1298-11459T=	NP_001258090.1:n.1298-11459T=
NM_001271162.1:c.8-11459T=	NP_001258091.1:n.8-11459T=
NR_073141.2:n.1783-11459T=
NR_073142.2:n.1782+22672T=
NR_073143.2:n.1783-11459T=
XM_006718858.2:c.1790-11459T=	XP_006718921.1:n.1790-11459T=
XR_947831.1:n.3362-11459T=
XM_006718858.3:c.1790-11459T=	XP_006718921.1:n.1790-11459T=
NM_001271162.2:c.8-11459T=	NP_001258091.1:n.8-11459T=
NR_073141.3:n.1797-11459T=
NR_073142.3:n.1796+22672T=
NR_073143.3:n.1797-11459T=