Canonical Allele Identifier: CA1995637139

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034535T= , CM000673.2:g.101034535T=	GRCh38
NC_000011.9:g.100905266T= , CM000673.1:g.100905266T=	GRCh37
NC_000011.8:g.100410476T=	NCBI36
NG_016475.1:g.100279A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4581A= MANE Select	ENSP00000325120.5:n.*4581A=
ENST00000325455.9:c.*4581A=	ENSP00000325120.5:n.*4581A=
NM_000926.4:c.*4581A= MANE Select	NP_000917.3:n.*4581A=
NM_001202474.3:c.*4581A=	NP_001189403.1:n.*4581A=
NM_001271161.2:c.*4581A=	NP_001258090.1:n.*4581A=
NM_001271162.1:c.*4581A=	NP_001258091.1:n.*4581A=
NR_073141.2:n.7324A=
NR_073142.2:n.7207A=
NR_073143.2:n.6939A=
NM_001271162.2:c.*4581A=	NP_001258091.1:n.*4581A=
NR_073141.3:n.7338A=
NR_073142.3:n.7221A=
NR_073143.3:n.6953A=