Canonical Allele Identifier: CA1995639246

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101039260T= , CM000673.2:g.101039260T=	GRCh38
NC_000011.9:g.100909991T= , CM000673.1:g.100909991T=	GRCh37
NC_000011.8:g.100415201T=	NCBI36
NG_016475.1:g.95554A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000926.4:c.2658A= MANE Select	NP_000917.3:p.Gln886=
ENST00000325455.10:c.2658A= MANE Select	ENSP00000325120.5:p.Gln886=
NM_001202474.3:c.2166A=	NP_001189403.1:p.Gln722=
NM_001271161.2:c.1860A=	NP_001258090.1:p.Gln620=
NM_001271162.1:c.876A=	NP_001258091.1:p.Gln292=
NM_001271162.2:c.876A=	NP_001258091.1:p.Gln292=
NR_073141.2:n.2599A=
NR_073141.3:n.2613A=
NR_073142.2:n.2482A=
NR_073142.3:n.2496A=
NR_073143.2:n.2214A=
NR_073143.3:n.2228A=
ENST00000263463.9:c.2352A=	ENSP00000263463.5:p.Gln784=
ENST00000325455.9:c.2658A=	ENSP00000325120.5:p.Gln886=
ENST00000526300.5:c.2221A=	ENSP00000436803.1:n.2221A=
ENST00000528960.5:c.2489A=	ENSP00000432914.1:n.2489A=
ENST00000533207.5:n.2025A=
ENST00000534013.5:c.876A=	ENSP00000436561.1:p.Gln292=
ENST00000534780.5:c.2606A=	ENSP00000432352.1:n.2606A=