Canonical Allele Identifier: CA1995648890

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101096840A= , CM000673.2:g.101096840A=	GRCh38
NC_000011.9:g.100967571A= , CM000673.1:g.100967571A=	GRCh37
NC_000011.8:g.100472781A=	NCBI36
NG_016475.1:g.37974T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.1790-4964T= MANE Select	ENSP00000325120.5:n.1790-4964T=
ENST00000263463.9:c.1790-4964T=	ENSP00000263463.5:n.1790-4964T=
ENST00000325455.9:c.1790-4964T=	ENSP00000325120.5:n.1790-4964T=
ENST00000526300.5:c.1790-4964T=	ENSP00000436803.1:n.1790-4964T=
ENST00000528960.5:c.1789+29167T=	ENSP00000432914.1:n.1789+29167T=
ENST00000534013.5:c.8-4964T=	ENSP00000436561.1:n.8-4964T=
ENST00000534780.5:c.1790-4964T=	ENSP00000432352.1:n.1790-4964T=
ENST00000617858.4:c.1790-4964T=	ENSP00000481227.1:n.1790-4964T=
ENST00000619228.2:c.1789+29167T=	ENSP00000482698.1:n.1789+29167T=
ENST00000632634.1:c.212-4964T=	ENSP00000487607.1:n.212-4964T=
NM_000926.4:c.1790-4964T= MANE Select	NP_000917.3:n.1790-4964T=
NM_001202474.3:c.1298-4964T=	NP_001189403.1:n.1298-4964T=
NM_001271161.2:c.1298-4964T=	NP_001258090.1:n.1298-4964T=
NM_001271162.1:c.8-4964T=	NP_001258091.1:n.8-4964T=
NR_073141.2:n.1783-4964T=
NR_073142.2:n.1782+29167T=
NR_073143.2:n.1783-4964T=
XM_006718858.2:c.1790-4964T=	XP_006718921.1:n.1790-4964T=
XR_947831.1:n.3362-4964T=
XM_006718858.3:c.1790-4964T=	XP_006718921.1:n.1790-4964T=
NM_001271162.2:c.8-4964T=	NP_001258091.1:n.8-4964T=
NR_073141.3:n.1797-4964T=
NR_073142.3:n.1796+29167T=
NR_073143.3:n.1797-4964T=