Canonical Allele Identifier: CA402344584

Gene: EPG5

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45882288C>A , CM000680.2:g.45882288C>A	GRCh38
NC_000018.9:g.43462253C>A , CM000680.1:g.43462253C>A	GRCh37
NC_000018.8:g.41716251C>A	NCBI36
NG_042838.1:g.90052G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020964.3:c.5504G>T MANE Select	NP_066015.2:p.Arg1835Met
ENST00000282041.11:c.5504G>T MANE Select	ENSP00000282041.4:p.Arg1835Met
NM_020964.2:c.5504G>T	NP_066015.2:p.Arg1835Met
ENST00000282041.9:c.5504G>T	ENSP00000282041.4:p.Arg1835Met
ENST00000585906.5:n.2283G>T
ENST00000586655.2:n.3765G>T
ENST00000587884.1:c.*1244G>T	ENSP00000466990.1:n.*1244G>T
ENST00000587884.2:c.5630G>T	ENSP00000466990.2:n.5630G>T
ENST00000587973.2:n.1369G>T
ENST00000590884.5:c.*99G>T	ENSP00000466403.1:n.*99G>T
ENST00000590884.6:c.5448G>T	ENSP00000466403.2:n.5448G>T
ENST00000592272.5:c.2129G>T	ENSP00000467464.1:p.Arg710Met
ENST00000592272.6:c.5504G>T	ENSP00000467464.2:p.Arg1835Met
ENST00000696481.1:n.2136G>T
ENST00000696482.1:c.5244G>T	ENSP00000512656.1:n.5244G>T
ENST00000696483.1:c.5504G>T	ENSP00000512657.1:p.Arg1835Met
ENST00000696484.1:c.5504G>T	ENSP00000512658.1:p.Arg1835Met
ENST00000696485.1:c.*99G>T	ENSP00000512659.1:n.*99G>T
ENST00000696489.1:c.5504G>T	ENSP00000512660.1:p.Arg1835Met
ENST00000696490.1:c.5504G>T	ENSP00000512661.1:p.Arg1835Met
XM_011526120.1:c.5531G>T	XP_011524422.1:p.Arg1844Met
XM_011526121.1:c.5531G>T	XP_011524423.1:p.Arg1844Met
XM_011526122.1:c.5504G>T	XP_011524424.1:p.Arg1835Met
XM_011526123.1:c.5531G>T	XP_011524425.1:p.Arg1844Met
XM_011526124.1:c.5531G>T	XP_011524426.1:p.Arg1844Met
XM_011526125.1:c.5390G>T	XP_011524427.1:p.Arg1797Met
XM_011526126.1:c.4466G>T	XP_011524428.1:p.Arg1489Met
XM_011526127.1:c.5531G>T	XP_011524429.1:p.Arg1844Met
XM_011526128.1:c.*99G>T	XP_011524430.1:n.*99G>T
XM_017025889.1:c.5504G>T	XP_016881378.1:p.Arg1835Met
XM_017025890.2:c.5504G>T	XP_016881379.1:p.Arg1835Met
XM_017025891.1:c.5363G>T	XP_016881380.1:p.Arg1788Met
XM_017025892.1:c.4439G>T	XP_016881381.1:p.Arg1480Met
XM_017025893.1:c.2129G>T	XP_016881382.1:p.Arg710Met
XR_001753256.1:n.5586G>T
XR_001753257.1:n.5530G>T
XR_935244.1:n.5604G>T