Canonical Allele Identifier: CA476501641

Gene: PGR

Linked Data

• gnomAD v4: 11-101051543-G-A
• MyVariant Identifiers: chr11:g.100922274G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051543G>A , CM000673.2:g.101051543G>A	GRCh38
NC_000011.9:g.100922274G>A , CM000673.1:g.100922274G>A	GRCh37
NC_000011.8:g.100427484G>A	NCBI36
NG_016475.1:g.83271C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2238C>T MANE Select	ENSP00000325120.5:p.Asp746=
ENST00000263463.9:c.1932C>T	ENSP00000263463.5:p.Asp644=
ENST00000325455.9:c.2238C>T	ENSP00000325120.5:p.Asp746=
ENST00000526300.5:c.1932C>T	ENSP00000436803.1:p.Asp644=
ENST00000528960.5:c.2121C>T	ENSP00000432914.1:p.Asp707=
ENST00000533207.5:n.1605C>T
ENST00000534013.5:c.456C>T	ENSP00000436561.1:p.Asp152=
ENST00000534780.5:c.2238C>T	ENSP00000432352.1:p.Asp746=
ENST00000617858.4:c.1932C>T	ENSP00000481227.1:p.Asp644=
ENST00000619228.2:c.2121C>T	ENSP00000482698.1:p.Asp707=
NM_000926.4:c.2238C>T MANE Select	NP_000917.3:p.Asp746=
NM_001202474.3:c.1746C>T	NP_001189403.1:p.Asp582=
NM_001271161.2:c.1440C>T	NP_001258090.1:p.Asp480=
NM_001271162.1:c.456C>T	NP_001258091.1:p.Asp152=
NR_073141.2:n.2231C>T
NR_073142.2:n.2114C>T
NR_073143.2:n.1925C>T
XM_006718858.2:c.2238C>T	XP_006718921.1:p.Asp746=
XR_947831.1:n.3919C>T
XM_006718858.3:c.2238C>T	XP_006718921.1:p.Asp746=
NM_001271162.2:c.456C>T	NP_001258091.1:p.Asp152=
NR_073141.3:n.2245C>T
NR_073142.3:n.2128C>T
NR_073143.3:n.1939C>T