Canonical Allele Identifier: CA476501557

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922157A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.2355T>C MANE Select	ENSP00000325120.5:p.Asn785=
ENST00000263463.9:c.2049T>C	ENSP00000263463.5:p.Asn683=
ENST00000325455.9:c.2355T>C	ENSP00000325120.5:p.Asn785=
ENST00000526300.5:c.2049T>C	ENSP00000436803.1:p.Asn683=
ENST00000528960.5:c.2238T>C	ENSP00000432914.1:p.Asn746=
ENST00000530764.1:n.45T>C
ENST00000533207.5:n.1722T>C
ENST00000534013.5:c.573T>C	ENSP00000436561.1:p.Asn191=
ENST00000534780.5:c.2355T>C	ENSP00000432352.1:p.Asn785=
ENST00000617858.4:c.2049T>C	ENSP00000481227.1:p.Asn683=
ENST00000619228.2:c.2238T>C	ENSP00000482698.1:p.Asn746=
NM_000926.4:c.2355T>C MANE Select	NP_000917.3:p.Asn785=
NM_001202474.3:c.1863T>C	NP_001189403.1:p.Asn621=
NM_001271161.2:c.1557T>C	NP_001258090.1:p.Asn519=
NM_001271162.1:c.573T>C	NP_001258091.1:p.Asn191=
NR_073141.2:n.2348T>C
NR_073142.2:n.2231T>C
NR_073143.2:n.2042T>C
XM_006718858.2:c.2355T>C	XP_006718921.1:p.Asn785=
XM_006718858.3:c.2355T>C	XP_006718921.1:p.Asn785=
NM_001271162.2:c.573T>C	NP_001258091.1:p.Asn191=
NR_073141.3:n.2362T>C
NR_073142.3:n.2245T>C
NR_073143.3:n.2056T>C