Canonical Allele Identifier: CA1995639171

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101039078A= , CM000673.2:g.101039078A=	GRCh38
NC_000011.9:g.100909809A= , CM000673.1:g.100909809A=	GRCh37
NC_000011.8:g.100415019A=	NCBI36
NG_016475.1:g.95736T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000926.4:c.*38T= MANE Select	NP_000917.3:n.*38T=
ENST00000325455.10:c.*38T= MANE Select	ENSP00000325120.5:n.*38T=
NM_001202474.3:c.*38T=	NP_001189403.1:n.*38T=
NM_001271161.2:c.*38T=	NP_001258090.1:n.*38T=
NM_001271162.1:c.*38T=	NP_001258091.1:n.*38T=
NM_001271162.2:c.*38T=	NP_001258091.1:n.*38T=
NR_073141.2:n.2781T=
NR_073141.3:n.2795T=
NR_073142.2:n.2664T=
NR_073142.3:n.2678T=
NR_073143.2:n.2396T=
NR_073143.3:n.2410T=
ENST00000325455.9:c.*38T=	ENSP00000325120.5:n.*38T=
ENST00000533207.5:n.2207T=
ENST00000534013.5:c.*38T=	ENSP00000436561.1:n.*38T=