Canonical Allele Identifier: CA503800787
Community Standard Title: NM_020964.3(EPG5):c.5412T>C (p.Asp1804=)
Gene: EPG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45882380A>G , CM000680.2:g.45882380A>G GRCh38
NC_000018.9:g.43462345A>G , CM000680.1:g.43462345A>G GRCh37
NC_000018.8:g.41716343A>G NCBI36
NG_042838.1:g.89960T>C

Transcript Alleles

HGVS Amino-acid Change
NM_020964.3:c.5412T>C MANE Select NP_066015.2:p.Asp1804=
ENST00000282041.11:c.5412T>C MANE Select ENSP00000282041.4:p.Asp1804=
NM_020964.2:c.5412T>C NP_066015.2:p.Asp1804=
ENST00000282041.9:c.5412T>C ENSP00000282041.4:p.Asp1804=
ENST00000585906.5:n.2191T>C
ENST00000586655.2:n.3673T>C
ENST00000587884.1:c.*1152T>C ENSP00000466990.1:n.*1152T>C
ENST00000587884.2:c.5538T>C ENSP00000466990.2:n.5538T>C
ENST00000587973.2:n.1277T>C
ENST00000590884.5:c.*7T>C ENSP00000466403.1:n.*7T>C
ENST00000590884.6:c.5356T>C ENSP00000466403.2:n.5356T>C
ENST00000592272.5:c.2037T>C ENSP00000467464.1:p.Asp679=
ENST00000592272.6:c.5412T>C ENSP00000467464.2:p.Asp1804=
ENST00000696481.1:n.2044T>C
ENST00000696482.1:c.5152T>C ENSP00000512656.1:n.5152T>C
ENST00000696483.1:c.5412T>C ENSP00000512657.1:p.Asp1804=
ENST00000696484.1:c.5412T>C ENSP00000512658.1:p.Asp1804=
ENST00000696485.1:c.*7T>C ENSP00000512659.1:n.*7T>C
ENST00000696489.1:c.5412T>C ENSP00000512660.1:p.Asp1804=
ENST00000696490.1:c.5412T>C ENSP00000512661.1:p.Asp1804=
XM_011526120.1:c.5439T>C XP_011524422.1:p.Asp1813=
XM_011526121.1:c.5439T>C XP_011524423.1:p.Asp1813=
XM_011526122.1:c.5412T>C XP_011524424.1:p.Asp1804=
XM_011526123.1:c.5439T>C XP_011524425.1:p.Asp1813=
XM_011526124.1:c.5439T>C XP_011524426.1:p.Asp1813=
XM_011526125.1:c.5298T>C XP_011524427.1:p.Asp1766=
XM_011526126.1:c.4374T>C XP_011524428.1:p.Asp1458=
XM_011526127.1:c.5439T>C XP_011524429.1:p.Asp1813=
XM_011526128.1:c.*7T>C XP_011524430.1:n.*7T>C
XM_017025889.1:c.5412T>C XP_016881378.1:p.Asp1804=
XM_017025890.2:c.5412T>C XP_016881379.1:p.Asp1804=
XM_017025891.1:c.5271T>C XP_016881380.1:p.Asp1757=
XM_017025892.1:c.4347T>C XP_016881381.1:p.Asp1449=
XM_017025893.1:c.2037T>C XP_016881382.1:p.Asp679=
XR_001753256.1:n.5494T>C
XR_001753257.1:n.5438T>C
XR_935244.1:n.5512T>C