Canonical Allele Identifier: CA1995635503

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101030742A= , CM000673.2:g.101030742A=	GRCh38
NC_000011.9:g.100901473A= , CM000673.1:g.100901473A=	GRCh37
NC_000011.8:g.100406683A=	NCBI36
NG_016475.1:g.104072T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000926.4:c.*8374T= MANE Select	NP_000917.3:n.*8374T=
ENST00000325455.10:c.*8374T= MANE Select	ENSP00000325120.5:n.*8374T=
NM_001202474.3:c.*8374T=	NP_001189403.1:n.*8374T=
NM_001271161.2:c.*8374T=	NP_001258090.1:n.*8374T=
NM_001271162.1:c.*8374T=	NP_001258091.1:n.*8374T=
NM_001271162.2:c.*8374T=	NP_001258091.1:n.*8374T=
NR_073141.2:n.11117T=
NR_073141.3:n.11131T=
NR_073142.2:n.11000T=
NR_073142.3:n.11014T=
NR_073143.2:n.10732T=
NR_073143.3:n.10746T=
ENST00000325455.9:c.*8374T=	ENSP00000325120.5:n.*8374T=