Canonical Allele Identifier: CA382436152

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051471G>T , CM000673.2:g.101051471G>T	GRCh38
NC_000011.9:g.100922202G>T , CM000673.1:g.100922202G>T	GRCh37
NC_000011.8:g.100427412G>T	NCBI36
NG_016475.1:g.83343C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000926.4:c.2310C>A MANE Select	NP_000917.3:p.His770Gln
ENST00000325455.10:c.2310C>A MANE Select	ENSP00000325120.5:p.His770Gln
NM_001202474.3:c.1818C>A	NP_001189403.1:p.His606Gln
NM_001271161.2:c.1512C>A	NP_001258090.1:p.His504Gln
NM_001271162.1:c.528C>A	NP_001258091.1:p.His176Gln
NM_001271162.2:c.528C>A	NP_001258091.1:p.His176Gln
NR_073141.2:n.2303C>A
NR_073141.3:n.2317C>A
NR_073142.2:n.2186C>A
NR_073142.3:n.2200C>A
NR_073143.2:n.1997C>A
NR_073143.3:n.2011C>A
ENST00000263463.9:c.2004C>A	ENSP00000263463.5:p.His668Gln
ENST00000325455.9:c.2310C>A	ENSP00000325120.5:p.His770Gln
ENST00000526300.5:c.2004C>A	ENSP00000436803.1:p.His668Gln
ENST00000528960.5:c.2193C>A	ENSP00000432914.1:p.His731Gln
ENST00000533207.5:n.1677C>A
ENST00000534013.5:c.528C>A	ENSP00000436561.1:p.His176Gln
ENST00000534780.5:c.2310C>A	ENSP00000432352.1:p.His770Gln
ENST00000617858.4:c.2004C>A	ENSP00000481227.1:p.His668Gln
ENST00000619228.2:c.2193C>A	ENSP00000482698.1:p.His731Gln
XM_006718858.2:c.2310C>A	XP_006718921.1:p.His770Gln
XM_006718858.3:c.2310C>A	XP_006718921.1:p.His770Gln