Canonical Allele Identifier: CA402344577

Gene: EPG5

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45882285A>T , CM000680.2:g.45882285A>T	GRCh38
NC_000018.9:g.43462250A>T , CM000680.1:g.43462250A>T	GRCh37
NC_000018.8:g.41716248A>T	NCBI36
NG_042838.1:g.90055T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020964.3:c.5507T>A MANE Select	NP_066015.2:p.Leu1836Gln
ENST00000282041.11:c.5507T>A MANE Select	ENSP00000282041.4:p.Leu1836Gln
NM_020964.2:c.5507T>A	NP_066015.2:p.Leu1836Gln
ENST00000282041.9:c.5507T>A	ENSP00000282041.4:p.Leu1836Gln
ENST00000585906.5:n.2286T>A
ENST00000586655.2:n.3768T>A
ENST00000587884.1:c.*1247T>A	ENSP00000466990.1:n.*1247T>A
ENST00000587884.2:c.5633T>A	ENSP00000466990.2:n.5633T>A
ENST00000587973.2:n.1372T>A
ENST00000590884.5:c.*102T>A	ENSP00000466403.1:n.*102T>A
ENST00000590884.6:c.5451T>A	ENSP00000466403.2:n.5451T>A
ENST00000592272.5:c.2132T>A	ENSP00000467464.1:p.Leu711Gln
ENST00000592272.6:c.5507T>A	ENSP00000467464.2:p.Leu1836Gln
ENST00000696481.1:n.2139T>A
ENST00000696482.1:c.5247T>A	ENSP00000512656.1:n.5247T>A
ENST00000696483.1:c.5507T>A	ENSP00000512657.1:p.Leu1836Gln
ENST00000696484.1:c.5507T>A	ENSP00000512658.1:p.Leu1836Gln
ENST00000696485.1:c.*102T>A	ENSP00000512659.1:n.*102T>A
ENST00000696489.1:c.5507T>A	ENSP00000512660.1:p.Leu1836Gln
ENST00000696490.1:c.5507T>A	ENSP00000512661.1:p.Leu1836Gln
XM_011526120.1:c.5534T>A	XP_011524422.1:p.Leu1845Gln
XM_011526121.1:c.5534T>A	XP_011524423.1:p.Leu1845Gln
XM_011526122.1:c.5507T>A	XP_011524424.1:p.Leu1836Gln
XM_011526123.1:c.5534T>A	XP_011524425.1:p.Leu1845Gln
XM_011526124.1:c.5534T>A	XP_011524426.1:p.Leu1845Gln
XM_011526125.1:c.5393T>A	XP_011524427.1:p.Leu1798Gln
XM_011526126.1:c.4469T>A	XP_011524428.1:p.Leu1490Gln
XM_011526127.1:c.5534T>A	XP_011524429.1:p.Leu1845Gln
XM_011526128.1:c.*102T>A	XP_011524430.1:n.*102T>A
XM_017025889.1:c.5507T>A	XP_016881378.1:p.Leu1836Gln
XM_017025890.2:c.5507T>A	XP_016881379.1:p.Leu1836Gln
XM_017025891.1:c.5366T>A	XP_016881380.1:p.Leu1789Gln
XM_017025892.1:c.4442T>A	XP_016881381.1:p.Leu1481Gln
XM_017025893.1:c.2132T>A	XP_016881382.1:p.Leu711Gln
XR_001753256.1:n.5589T>A
XR_001753257.1:n.5533T>A
XR_935244.1:n.5607T>A