Canonical Allele Identifier: CA299760271
Gene: EPG5 HGNC NCBI

Linked Data

dbSNP Id: rs773767816

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45910525C>G , CM000680.2:g.45910525C>G GRCh38
NC_000018.9:g.43490490C>G , CM000680.1:g.43490490C>G GRCh37
NC_000018.8:g.41744488C>G NCBI36
NG_042838.1:g.61815G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000586655.2:n.2385G>C
ENST00000587884.2:c.4201G>C ENSP00000466990.2:p.Val1401Leu
ENST00000590884.6:c.4201G>C ENSP00000466403.2:p.Val1401Leu
ENST00000592272.6:c.4201G>C ENSP00000467464.2:p.Val1401Leu
ENST00000696482.1:c.3941G>C ENSP00000512656.1:n.3941G>C
ENST00000696483.1:c.4201G>C ENSP00000512657.1:p.Val1401Leu
ENST00000696484.1:c.4201G>C ENSP00000512658.1:p.Val1401Leu
ENST00000696485.1:c.4201G>C ENSP00000512659.1:p.Val1401Leu
ENST00000696489.1:c.4201G>C ENSP00000512660.1:p.Val1401Leu
ENST00000696490.1:c.4201G>C ENSP00000512661.1:p.Val1401Leu
ENST00000282041.11:c.4201G>C MANE Select ENSP00000282041.4:p.Val1401Leu
ENST00000282041.9:c.4201G>C ENSP00000282041.4:p.Val1401Leu
ENST00000585906.5:n.980G>C
ENST00000587884.1:c.826G>C ENSP00000466990.1:p.Val276Leu
ENST00000587974.1:n.4236G>C
ENST00000590884.5:c.826G>C ENSP00000466403.1:p.Val276Leu
ENST00000592272.5:c.826G>C ENSP00000467464.1:p.Val276Leu
NM_020964.2:c.4201G>C NP_066015.2:p.Val1401Leu
XM_011526120.1:c.4228G>C XP_011524422.1:p.Val1410Leu
XM_011526121.1:c.4228G>C XP_011524423.1:p.Val1410Leu
XM_011526122.1:c.4201G>C XP_011524424.1:p.Val1401Leu
XM_011526123.1:c.4228G>C XP_011524425.1:p.Val1410Leu
XM_011526124.1:c.4228G>C XP_011524426.1:p.Val1410Leu
XM_011526125.1:c.4087G>C XP_011524427.1:p.Val1363Leu
XM_011526126.1:c.3163G>C XP_011524428.1:p.Val1055Leu
XM_011526127.1:c.4228G>C XP_011524429.1:p.Val1410Leu
XM_011526128.1:c.4228G>C XP_011524430.1:p.Val1410Leu
XR_935244.1:n.4301G>C
NM_020964.3:c.4201G>C MANE Select NP_066015.2:p.Val1401Leu
XM_017025889.1:c.4201G>C XP_016881378.1:p.Val1401Leu
XM_017025890.2:c.4201G>C XP_016881379.1:p.Val1401Leu
XM_017025891.1:c.4060G>C XP_016881380.1:p.Val1354Leu
XM_017025892.1:c.3136G>C XP_016881381.1:p.Val1046Leu
XM_017025893.1:c.826G>C XP_016881382.1:p.Val276Leu
XR_001753256.1:n.4283G>C
XR_001753257.1:n.4283G>C