Canonical Allele Identifier: CA1995654086

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062626C= , CM000673.2:g.101062626C=	GRCh38
NC_000011.9:g.100933357C= , CM000673.1:g.100933357C=	GRCh37
NC_000011.8:g.100438567C=	NCBI36
NG_016475.1:g.72188G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2033G= MANE Select	ENSP00000325120.5:p.Gly678=
ENST00000263463.9:c.1907-11058G=	ENSP00000263463.5:n.1907-11058G=
ENST00000325455.9:c.2033G=	ENSP00000325120.5:p.Gly678=
ENST00000526300.5:c.1907-11058G=	ENSP00000436803.1:n.1907-11058G=
ENST00000528960.5:c.1916G=	ENSP00000432914.1:p.Gly639=
ENST00000533207.5:n.1400G=
ENST00000534013.5:c.251G=	ENSP00000436561.1:p.Gly84=
ENST00000534780.5:c.2033G=	ENSP00000432352.1:p.Gly678=
ENST00000617858.4:c.1907-11058G=	ENSP00000481227.1:n.1907-11058G=
ENST00000619228.2:c.1916G=	ENSP00000482698.1:p.Gly639=
ENST00000632634.1:c.455G=	ENSP00000487607.1:p.Gly152=
NM_000926.4:c.2033G= MANE Select	NP_000917.3:p.Gly678=
NM_001202474.3:c.1541G=	NP_001189403.1:p.Gly514=
NM_001271161.2:c.1415-11058G=	NP_001258090.1:n.1415-11058G=
NM_001271162.1:c.251G=	NP_001258091.1:p.Gly84=
NR_073141.2:n.2026G=
NR_073142.2:n.1909G=
NR_073143.2:n.1900-11058G=
XM_006718858.2:c.2033G=	XP_006718921.1:p.Gly678=
XR_947831.1:n.3605G=
XM_006718858.3:c.2033G=	XP_006718921.1:p.Gly678=
NM_001271162.2:c.251G=	NP_001258091.1:p.Gly84=
NR_073141.3:n.2040G=
NR_073142.3:n.1923G=
NR_073143.3:n.1914-11058G=