Canonical Allele Identifier: CA402344579

Gene: EPG5

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_020964.3:c.5507T>G MANE Select	NP_066015.2:p.Leu1836Arg
ENST00000282041.11:c.5507T>G MANE Select	ENSP00000282041.4:p.Leu1836Arg
NM_020964.2:c.5507T>G	NP_066015.2:p.Leu1836Arg
ENST00000282041.9:c.5507T>G	ENSP00000282041.4:p.Leu1836Arg
ENST00000585906.5:n.2286T>G
ENST00000586655.2:n.3768T>G
ENST00000587884.1:c.*1247T>G	ENSP00000466990.1:n.*1247T>G
ENST00000587884.2:c.5633T>G	ENSP00000466990.2:n.5633T>G
ENST00000587973.2:n.1372T>G
ENST00000590884.5:c.*102T>G	ENSP00000466403.1:n.*102T>G
ENST00000590884.6:c.5451T>G	ENSP00000466403.2:n.5451T>G
ENST00000592272.5:c.2132T>G	ENSP00000467464.1:p.Leu711Arg
ENST00000592272.6:c.5507T>G	ENSP00000467464.2:p.Leu1836Arg
ENST00000696481.1:n.2139T>G
ENST00000696482.1:c.5247T>G	ENSP00000512656.1:n.5247T>G
ENST00000696483.1:c.5507T>G	ENSP00000512657.1:p.Leu1836Arg
ENST00000696484.1:c.5507T>G	ENSP00000512658.1:p.Leu1836Arg
ENST00000696485.1:c.*102T>G	ENSP00000512659.1:n.*102T>G
ENST00000696489.1:c.5507T>G	ENSP00000512660.1:p.Leu1836Arg
ENST00000696490.1:c.5507T>G	ENSP00000512661.1:p.Leu1836Arg
XM_011526120.1:c.5534T>G	XP_011524422.1:p.Leu1845Arg
XM_011526121.1:c.5534T>G	XP_011524423.1:p.Leu1845Arg
XM_011526122.1:c.5507T>G	XP_011524424.1:p.Leu1836Arg
XM_011526123.1:c.5534T>G	XP_011524425.1:p.Leu1845Arg
XM_011526124.1:c.5534T>G	XP_011524426.1:p.Leu1845Arg
XM_011526125.1:c.5393T>G	XP_011524427.1:p.Leu1798Arg
XM_011526126.1:c.4469T>G	XP_011524428.1:p.Leu1490Arg
XM_011526127.1:c.5534T>G	XP_011524429.1:p.Leu1845Arg
XM_011526128.1:c.*102T>G	XP_011524430.1:n.*102T>G
XM_017025889.1:c.5507T>G	XP_016881378.1:p.Leu1836Arg
XM_017025890.2:c.5507T>G	XP_016881379.1:p.Leu1836Arg
XM_017025891.1:c.5366T>G	XP_016881380.1:p.Leu1789Arg
XM_017025892.1:c.4442T>G	XP_016881381.1:p.Leu1481Arg
XM_017025893.1:c.2132T>G	XP_016881382.1:p.Leu711Arg
XR_001753256.1:n.5589T>G
XR_001753257.1:n.5533T>G
XR_935244.1:n.5607T>G