Canonical Allele Identifier: CA382436051

Gene: PGR

Linked Data

• gnomAD v4: 11-101051426-A-T
• MyVariant Identifiers: chr11:g.100922157A>T (hg19) ; chr11:g.101051426A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051426A>T , CM000673.2:g.101051426A>T	GRCh38
NC_000011.9:g.100922157A>T , CM000673.1:g.100922157A>T	GRCh37
NC_000011.8:g.100427367A>T	NCBI36
NG_016475.1:g.83388T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.2355T>A MANE Select	ENSP00000325120.5:p.Asn785Lys
ENST00000263463.9:c.2049T>A	ENSP00000263463.5:p.Asn683Lys
ENST00000325455.9:c.2355T>A	ENSP00000325120.5:p.Asn785Lys
ENST00000526300.5:c.2049T>A	ENSP00000436803.1:p.Asn683Lys
ENST00000528960.5:c.2238T>A	ENSP00000432914.1:p.Asn746Lys
ENST00000530764.1:n.45T>A
ENST00000533207.5:n.1722T>A
ENST00000534013.5:c.573T>A	ENSP00000436561.1:p.Asn191Lys
ENST00000534780.5:c.2355T>A	ENSP00000432352.1:p.Asn785Lys
ENST00000617858.4:c.2049T>A	ENSP00000481227.1:p.Asn683Lys
ENST00000619228.2:c.2238T>A	ENSP00000482698.1:p.Asn746Lys
NM_000926.4:c.2355T>A MANE Select	NP_000917.3:p.Asn785Lys
NM_001202474.3:c.1863T>A	NP_001189403.1:p.Asn621Lys
NM_001271161.2:c.1557T>A	NP_001258090.1:p.Asn519Lys
NM_001271162.1:c.573T>A	NP_001258091.1:p.Asn191Lys
NR_073141.2:n.2348T>A
NR_073142.2:n.2231T>A
NR_073143.2:n.2042T>A
XM_006718858.2:c.2355T>A	XP_006718921.1:p.Asn785Lys
XM_006718858.3:c.2355T>A	XP_006718921.1:p.Asn785Lys
NM_001271162.2:c.573T>A	NP_001258091.1:p.Asn191Lys
NR_073141.3:n.2362T>A
NR_073142.3:n.2245T>A
NR_073143.3:n.2056T>A