Canonical Allele Identifier: CA1995703667

Gene: PGR PGR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101129484T= , CM000673.2:g.101129484T=	GRCh38
NC_000011.9:g.101000215T= , CM000673.1:g.101000215T=	GRCh37
NC_000011.8:g.100505425T=	NCBI36
NG_016475.1:g.5330A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.-414A= (PGR) MANE Select	ENSP00000325120.5:n.-414A=
ENST00000325455.9:c.-414A= (PGR)	ENSP00000325120.5:n.-414A=
ENST00000534013.5:c.-202A= (PGR)	ENSP00000436561.1:n.-202A=
ENST00000617858.4:c.-414A= (PGR)	ENSP00000481227.1:n.-414A=
ENST00000619228.2:c.-414A= (PGR)	ENSP00000482698.1:n.-414A=
NM_000926.4:c.-414A= (PGR) MANE Select	NP_000917.3:n.-414A=
NM_001271162.1:c.-202A= (PGR)	NP_001258091.1:n.-202A=
NR_073144.1:n.408T= (PGR-AS1)
XM_006718858.2:c.-414A= (PGR)	XP_006718921.1:n.-414A=
XM_011542869.1:c.-414A= (PGR)	XP_011541171.1:n.-414A=
XR_947831.1:n.1159A= (PGR)
XM_006718858.3:c.-414A= (PGR)	XP_006718921.1:n.-414A=
XM_011542869.2:c.-414A= (PGR)	XP_011541171.1:n.-414A=
NM_001271162.2:c.-202A= (PGR)	NP_001258091.1:n.-202A=