Canonical Allele Identifier: CA1995637258

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034782A= , CM000673.2:g.101034782A=	GRCh38
NC_000011.9:g.100905513A= , CM000673.1:g.100905513A=	GRCh37
NC_000011.8:g.100410723A=	NCBI36
NG_016475.1:g.100032T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4334T= MANE Select	ENSP00000325120.5:n.*4334T=
ENST00000325455.9:c.*4334T=	ENSP00000325120.5:n.*4334T=
NM_000926.4:c.*4334T= MANE Select	NP_000917.3:n.*4334T=
NM_001202474.3:c.*4334T=	NP_001189403.1:n.*4334T=
NM_001271161.2:c.*4334T=	NP_001258090.1:n.*4334T=
NM_001271162.1:c.*4334T=	NP_001258091.1:n.*4334T=
NR_073141.2:n.7077T=
NR_073142.2:n.6960T=
NR_073143.2:n.6692T=
NM_001271162.2:c.*4334T=	NP_001258091.1:n.*4334T=
NR_073141.3:n.7091T=
NR_073142.3:n.6974T=
NR_073143.3:n.6706T=