Canonical Allele Identifier: CA1995637217

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034694T= , CM000673.2:g.101034694T=	GRCh38
NC_000011.9:g.100905425T= , CM000673.1:g.100905425T=	GRCh37
NC_000011.8:g.100410635T=	NCBI36
NG_016475.1:g.100120A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4422A= MANE Select	ENSP00000325120.5:n.*4422A=
ENST00000325455.9:c.*4422A=	ENSP00000325120.5:n.*4422A=
NM_000926.4:c.*4422A= MANE Select	NP_000917.3:n.*4422A=
NM_001202474.3:c.*4422A=	NP_001189403.1:n.*4422A=
NM_001271161.2:c.*4422A=	NP_001258090.1:n.*4422A=
NM_001271162.1:c.*4422A=	NP_001258091.1:n.*4422A=
NR_073141.2:n.7165A=
NR_073142.2:n.7048A=
NR_073143.2:n.6780A=
NM_001271162.2:c.*4422A=	NP_001258091.1:n.*4422A=
NR_073141.3:n.7179A=
NR_073142.3:n.7062A=
NR_073143.3:n.6794A=