Canonical Allele Identifier: CA382437109

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100933397C>T (hg19) ; chr11:g.101062666C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062666C>T , CM000673.2:g.101062666C>T	GRCh38
NC_000011.9:g.100933397C>T , CM000673.1:g.100933397C>T	GRCh37
NC_000011.8:g.100438607C>T	NCBI36
NG_016475.1:g.72148G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.1993G>A MANE Select	ENSP00000325120.5:p.Glu665Lys
ENST00000263463.9:c.1907-11098G>A	ENSP00000263463.5:n.1907-11098G>A
ENST00000325455.9:c.1993G>A	ENSP00000325120.5:p.Glu665Lys
ENST00000526300.5:c.1907-11098G>A	ENSP00000436803.1:n.1907-11098G>A
ENST00000528960.5:c.1876G>A	ENSP00000432914.1:p.Glu626Lys
ENST00000533207.5:n.1360G>A
ENST00000534013.5:c.211G>A	ENSP00000436561.1:p.Glu71Lys
ENST00000534780.5:c.1993G>A	ENSP00000432352.1:p.Glu665Lys
ENST00000617858.4:c.1907-11098G>A	ENSP00000481227.1:n.1907-11098G>A
ENST00000619228.2:c.1876G>A	ENSP00000482698.1:p.Glu626Lys
ENST00000632634.1:c.415G>A	ENSP00000487607.1:p.Glu139Lys
NM_000926.4:c.1993G>A MANE Select	NP_000917.3:p.Glu665Lys
NM_001202474.3:c.1501G>A	NP_001189403.1:p.Glu501Lys
NM_001271161.2:c.1415-11098G>A	NP_001258090.1:n.1415-11098G>A
NM_001271162.1:c.211G>A	NP_001258091.1:p.Glu71Lys
NR_073141.2:n.1986G>A
NR_073142.2:n.1869G>A
NR_073143.2:n.1900-11098G>A
XM_006718858.2:c.1993G>A	XP_006718921.1:p.Glu665Lys
XR_947831.1:n.3565G>A
XM_006718858.3:c.1993G>A	XP_006718921.1:p.Glu665Lys
NM_001271162.2:c.211G>A	NP_001258091.1:p.Glu71Lys
NR_073141.3:n.2000G>A
NR_073142.3:n.1883G>A
NR_073143.3:n.1914-11098G>A