Canonical Allele Identifier: CA1995637101

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034415G= , CM000673.2:g.101034415G=	GRCh38
NC_000011.9:g.100905146G= , CM000673.1:g.100905146G=	GRCh37
NC_000011.8:g.100410356G=	NCBI36
NG_016475.1:g.100399C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4701C= MANE Select	ENSP00000325120.5:n.*4701C=
ENST00000325455.9:c.*4701C=	ENSP00000325120.5:n.*4701C=
NM_000926.4:c.*4701C= MANE Select	NP_000917.3:n.*4701C=
NM_001202474.3:c.*4701C=	NP_001189403.1:n.*4701C=
NM_001271161.2:c.*4701C=	NP_001258090.1:n.*4701C=
NM_001271162.1:c.*4701C=	NP_001258091.1:n.*4701C=
NR_073141.2:n.7444C=
NR_073142.2:n.7327C=
NR_073143.2:n.7059C=
NM_001271162.2:c.*4701C=	NP_001258091.1:n.*4701C=
NR_073141.3:n.7458C=
NR_073142.3:n.7341C=
NR_073143.3:n.7073C=