Canonical Allele Identifier: CA382437048
Gene: PGR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101062649G>C , CM000673.2:g.101062649G>C GRCh38
NC_000011.9:g.100933380G>C , CM000673.1:g.100933380G>C GRCh37
NC_000011.8:g.100438590G>C NCBI36
NG_016475.1:g.72165C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.2010C>G MANE Select ENSP00000325120.5:p.Ser670Arg
ENST00000263463.9:c.1907-11081C>G ENSP00000263463.5:n.1907-11081C>G
ENST00000325455.9:c.2010C>G ENSP00000325120.5:p.Ser670Arg
ENST00000526300.5:c.1907-11081C>G ENSP00000436803.1:n.1907-11081C>G
ENST00000528960.5:c.1893C>G ENSP00000432914.1:p.Ser631Arg
ENST00000533207.5:n.1377C>G
ENST00000534013.5:c.228C>G ENSP00000436561.1:p.Ser76Arg
ENST00000534780.5:c.2010C>G ENSP00000432352.1:p.Ser670Arg
ENST00000617858.4:c.1907-11081C>G ENSP00000481227.1:n.1907-11081C>G
ENST00000619228.2:c.1893C>G ENSP00000482698.1:p.Ser631Arg
ENST00000632634.1:c.432C>G ENSP00000487607.1:p.Ser144Arg
NM_000926.4:c.2010C>G MANE Select NP_000917.3:p.Ser670Arg
NM_001202474.3:c.1518C>G NP_001189403.1:p.Ser506Arg
NM_001271161.2:c.1415-11081C>G NP_001258090.1:n.1415-11081C>G
NM_001271162.1:c.228C>G NP_001258091.1:p.Ser76Arg
NR_073141.2:n.2003C>G
NR_073142.2:n.1886C>G
NR_073143.2:n.1900-11081C>G
XM_006718858.2:c.2010C>G XP_006718921.1:p.Ser670Arg
XR_947831.1:n.3582C>G
XM_006718858.3:c.2010C>G XP_006718921.1:p.Ser670Arg
NM_001271162.2:c.228C>G NP_001258091.1:p.Ser76Arg
NR_073141.3:n.2017C>G
NR_073142.3:n.1900C>G
NR_073143.3:n.1914-11081C>G