Canonical Allele Identifier: CA1995637342

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101035002A= , CM000673.2:g.101035002A=	GRCh38
NC_000011.9:g.100905733A= , CM000673.1:g.100905733A=	GRCh37
NC_000011.8:g.100410943A=	NCBI36
NG_016475.1:g.99812T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4114T= MANE Select	ENSP00000325120.5:n.*4114T=
ENST00000325455.9:c.*4114T=	ENSP00000325120.5:n.*4114T=
NM_000926.4:c.*4114T= MANE Select	NP_000917.3:n.*4114T=
NM_001202474.3:c.*4114T=	NP_001189403.1:n.*4114T=
NM_001271161.2:c.*4114T=	NP_001258090.1:n.*4114T=
NM_001271162.1:c.*4114T=	NP_001258091.1:n.*4114T=
NR_073141.2:n.6857T=
NR_073142.2:n.6740T=
NR_073143.2:n.6472T=
NM_001271162.2:c.*4114T=	NP_001258091.1:n.*4114T=
NR_073141.3:n.6871T=
NR_073142.3:n.6754T=
NR_073143.3:n.6486T=