Canonical Allele Identifier: CA1995637235

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034731C= , CM000673.2:g.101034731C=	GRCh38
NC_000011.9:g.100905462C= , CM000673.1:g.100905462C=	GRCh37
NC_000011.8:g.100410672C=	NCBI36
NG_016475.1:g.100083G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4385G= MANE Select	ENSP00000325120.5:n.*4385G=
ENST00000325455.9:c.*4385G=	ENSP00000325120.5:n.*4385G=
NM_000926.4:c.*4385G= MANE Select	NP_000917.3:n.*4385G=
NM_001202474.3:c.*4385G=	NP_001189403.1:n.*4385G=
NM_001271161.2:c.*4385G=	NP_001258090.1:n.*4385G=
NM_001271162.1:c.*4385G=	NP_001258091.1:n.*4385G=
NR_073141.2:n.7128G=
NR_073142.2:n.7011G=
NR_073143.2:n.6743G=
NM_001271162.2:c.*4385G=	NP_001258091.1:n.*4385G=
NR_073141.3:n.7142G=
NR_073142.3:n.7025G=
NR_073143.3:n.6757G=