Canonical Allele Identifier: CA402345001
Community Standard Title: NM_020964.3(EPG5):c.5318A>G (p.Gln1773Arg)
Gene: EPG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45882474T>C , CM000680.2:g.45882474T>C GRCh38
NC_000018.9:g.43462439T>C , CM000680.1:g.43462439T>C GRCh37
NC_000018.8:g.41716437T>C NCBI36
NG_042838.1:g.89866A>G

Transcript Alleles

HGVS Amino-acid Change
NM_020964.3:c.5318A>G MANE Select NP_066015.2:p.Gln1773Arg
ENST00000282041.11:c.5318A>G MANE Select ENSP00000282041.4:p.Gln1773Arg
NM_020964.2:c.5318A>G NP_066015.2:p.Gln1773Arg
ENST00000282041.9:c.5318A>G ENSP00000282041.4:p.Gln1773Arg
ENST00000585906.5:n.2097A>G
ENST00000586655.2:n.3622-43A>G
ENST00000587884.1:c.*1058A>G ENSP00000466990.1:n.*1058A>G
ENST00000587884.2:c.5444A>G ENSP00000466990.2:n.5444A>G
ENST00000587973.2:n.1183A>G
ENST00000590884.5:c.1930-43A>G ENSP00000466403.1:n.1930-43A>G
ENST00000590884.6:c.5305-43A>G ENSP00000466403.2:n.5305-43A>G
ENST00000592272.5:c.1943A>G ENSP00000467464.1:p.Gln648Arg
ENST00000592272.6:c.5318A>G ENSP00000467464.2:p.Gln1773Arg
ENST00000696481.1:n.1950A>G
ENST00000696482.1:c.5058A>G ENSP00000512656.1:n.5058A>G
ENST00000696483.1:c.5318A>G ENSP00000512657.1:p.Gln1773Arg
ENST00000696484.1:c.5318A>G ENSP00000512658.1:p.Gln1773Arg
ENST00000696485.1:c.5305-43A>G ENSP00000512659.1:n.5305-43A>G
ENST00000696489.1:c.5318A>G ENSP00000512660.1:p.Gln1773Arg
ENST00000696490.1:c.5318A>G ENSP00000512661.1:p.Gln1773Arg
XM_011526120.1:c.5345A>G XP_011524422.1:p.Gln1782Arg
XM_011526121.1:c.5345A>G XP_011524423.1:p.Gln1782Arg
XM_011526122.1:c.5318A>G XP_011524424.1:p.Gln1773Arg
XM_011526123.1:c.5345A>G XP_011524425.1:p.Gln1782Arg
XM_011526124.1:c.5345A>G XP_011524426.1:p.Gln1782Arg
XM_011526125.1:c.5204A>G XP_011524427.1:p.Gln1735Arg
XM_011526126.1:c.4280A>G XP_011524428.1:p.Gln1427Arg
XM_011526127.1:c.5345A>G XP_011524429.1:p.Gln1782Arg
XM_011526128.1:c.5332-43A>G XP_011524430.1:n.5332-43A>G
XM_017025889.1:c.5318A>G XP_016881378.1:p.Gln1773Arg
XM_017025890.2:c.5318A>G XP_016881379.1:p.Gln1773Arg
XM_017025891.1:c.5177A>G XP_016881380.1:p.Gln1726Arg
XM_017025892.1:c.4253A>G XP_016881381.1:p.Gln1418Arg
XM_017025893.1:c.1943A>G XP_016881382.1:p.Gln648Arg
XR_001753256.1:n.5400A>G
XR_001753257.1:n.5387-43A>G
XR_935244.1:n.5418A>G