Canonical Allele Identifier: CA1995703660

Gene: PGR PGR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101129483C= , CM000673.2:g.101129483C=	GRCh38
NC_000011.9:g.101000214C= , CM000673.1:g.101000214C=	GRCh37
NC_000011.8:g.100505424C=	NCBI36
NG_016475.1:g.5331G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000926.4:c.-413G= (PGR) MANE Select	NP_000917.3:n.-413G=
ENST00000325455.10:c.-413G= (PGR) MANE Select	ENSP00000325120.5:n.-413G=
NM_001271162.1:c.-201G= (PGR)	NP_001258091.1:n.-201G=
NM_001271162.2:c.-201G= (PGR)	NP_001258091.1:n.-201G=
NR_073144.1:n.407C= (PGR-AS1)
ENST00000325455.9:c.-413G= (PGR)	ENSP00000325120.5:n.-413G=
ENST00000534013.5:c.-201G= (PGR)	ENSP00000436561.1:n.-201G=
ENST00000617858.4:c.-413G= (PGR)	ENSP00000481227.1:n.-413G=
ENST00000619228.2:c.-413G= (PGR)	ENSP00000482698.1:n.-413G=
XM_006718858.2:c.-413G= (PGR)	XP_006718921.1:n.-413G=
XM_006718858.3:c.-413G= (PGR)	XP_006718921.1:n.-413G=
XM_011542869.1:c.-413G= (PGR)	XP_011541171.1:n.-413G=
XM_011542869.2:c.-413G= (PGR)	XP_011541171.1:n.-413G=
XR_947831.1:n.1160G= (PGR)