Canonical Allele Identifier: CA402339907

Gene: EPG5

Linked Data

• MyVariant Identifiers: chr18:g.43490539G>T (hg19) ; chr18:g.45910574G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45910574G>T , CM000680.2:g.45910574G>T	GRCh38
NC_000018.9:g.43490539G>T , CM000680.1:g.43490539G>T	GRCh37
NC_000018.8:g.41744537G>T	NCBI36
NG_042838.1:g.61766C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586655.2:n.2336C>A
ENST00000587884.2:c.4152C>A	ENSP00000466990.2:p.His1384Gln
ENST00000590884.6:c.4152C>A	ENSP00000466403.2:p.His1384Gln
ENST00000592272.6:c.4152C>A	ENSP00000467464.2:p.His1384Gln
ENST00000696482.1:c.3892C>A	ENSP00000512656.1:n.3892C>A
ENST00000696483.1:c.4152C>A	ENSP00000512657.1:p.His1384Gln
ENST00000696484.1:c.4152C>A	ENSP00000512658.1:p.His1384Gln
ENST00000696485.1:c.4152C>A	ENSP00000512659.1:p.His1384Gln
ENST00000696489.1:c.4152C>A	ENSP00000512660.1:p.His1384Gln
ENST00000696490.1:c.4152C>A	ENSP00000512661.1:p.His1384Gln
ENST00000282041.11:c.4152C>A MANE Select	ENSP00000282041.4:p.His1384Gln
ENST00000282041.9:c.4152C>A	ENSP00000282041.4:p.His1384Gln
ENST00000585906.5:n.931C>A
ENST00000587884.1:c.777C>A	ENSP00000466990.1:p.His259Gln
ENST00000587974.1:n.4187C>A
ENST00000590884.5:c.777C>A	ENSP00000466403.1:p.His259Gln
ENST00000592272.5:c.777C>A	ENSP00000467464.1:p.His259Gln
NM_020964.2:c.4152C>A	NP_066015.2:p.His1384Gln
XM_011526120.1:c.4179C>A	XP_011524422.1:p.His1393Gln
XM_011526121.1:c.4179C>A	XP_011524423.1:p.His1393Gln
XM_011526122.1:c.4152C>A	XP_011524424.1:p.His1384Gln
XM_011526123.1:c.4179C>A	XP_011524425.1:p.His1393Gln
XM_011526124.1:c.4179C>A	XP_011524426.1:p.His1393Gln
XM_011526125.1:c.4038C>A	XP_011524427.1:p.His1346Gln
XM_011526126.1:c.3114C>A	XP_011524428.1:p.His1038Gln
XM_011526127.1:c.4179C>A	XP_011524429.1:p.His1393Gln
XM_011526128.1:c.4179C>A	XP_011524430.1:p.His1393Gln
XR_935244.1:n.4252C>A
NM_020964.3:c.4152C>A MANE Select	NP_066015.2:p.His1384Gln
XM_017025889.1:c.4152C>A	XP_016881378.1:p.His1384Gln
XM_017025890.2:c.4152C>A	XP_016881379.1:p.His1384Gln
XM_017025891.1:c.4011C>A	XP_016881380.1:p.His1337Gln
XM_017025892.1:c.3087C>A	XP_016881381.1:p.His1029Gln
XM_017025893.1:c.777C>A	XP_016881382.1:p.His259Gln
XR_001753256.1:n.4234C>A
XR_001753257.1:n.4234C>A