Canonical Allele Identifier: CA382436179

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922214T>A (hg19) ; chr11:g.101051483T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051483T>A , CM000673.2:g.101051483T>A	GRCh38
NC_000011.9:g.100922214T>A , CM000673.1:g.100922214T>A	GRCh37
NC_000011.8:g.100427424T>A	NCBI36
NG_016475.1:g.83331A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2298A>T MANE Select	ENSP00000325120.5:p.Arg766Ser
ENST00000263463.9:c.1992A>T	ENSP00000263463.5:p.Arg664Ser
ENST00000325455.9:c.2298A>T	ENSP00000325120.5:p.Arg766Ser
ENST00000526300.5:c.1992A>T	ENSP00000436803.1:p.Arg664Ser
ENST00000528960.5:c.2181A>T	ENSP00000432914.1:p.Arg727Ser
ENST00000533207.5:n.1665A>T
ENST00000534013.5:c.516A>T	ENSP00000436561.1:p.Arg172Ser
ENST00000534780.5:c.2298A>T	ENSP00000432352.1:p.Arg766Ser
ENST00000617858.4:c.1992A>T	ENSP00000481227.1:p.Arg664Ser
ENST00000619228.2:c.2181A>T	ENSP00000482698.1:p.Arg727Ser
NM_000926.4:c.2298A>T MANE Select	NP_000917.3:p.Arg766Ser
NM_001202474.3:c.1806A>T	NP_001189403.1:p.Arg602Ser
NM_001271161.2:c.1500A>T	NP_001258090.1:p.Arg500Ser
NM_001271162.1:c.516A>T	NP_001258091.1:p.Arg172Ser
NR_073141.2:n.2291A>T
NR_073142.2:n.2174A>T
NR_073143.2:n.1985A>T
XM_006718858.2:c.2298A>T	XP_006718921.1:p.Arg766Ser
XM_006718858.3:c.2298A>T	XP_006718921.1:p.Arg766Ser
NM_001271162.2:c.516A>T	NP_001258091.1:p.Arg172Ser
NR_073141.3:n.2305A>T
NR_073142.3:n.2188A>T
NR_073143.3:n.1999A>T