Canonical Allele Identifier: CA2641629235

Gene: EPG5

Linked Data

• gnomAD v4: 18-45910561-C-CAGGGGTGCCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45910564_45910574dup , CM000680.2:g.45910564_45910574dup	GRCh38
NC_000018.9:g.43490529_43490539dup , CM000680.1:g.43490529_43490539dup	GRCh37
NC_000018.8:g.41744527_41744537dup	NCBI36
NG_042838.1:g.61768_61778dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586655.2:n.2338_2348dup
ENST00000587884.2:c.4154_4164dup	ENSP00000466990.2:p.Gly1389LeufsTer7
ENST00000590884.6:c.4154_4164dup	ENSP00000466403.2:p.Gly1389LeufsTer7
ENST00000592272.6:c.4154_4164dup	ENSP00000467464.2:p.Gly1389LeufsTer7
ENST00000696482.1:c.3894_3904dup	ENSP00000512656.1:n.3894_3904dup
ENST00000696483.1:c.4154_4164dup	ENSP00000512657.1:p.Gly1389LeufsTer7
ENST00000696484.1:c.4154_4164dup	ENSP00000512658.1:p.Gly1389LeufsTer7
ENST00000696485.1:c.4154_4164dup	ENSP00000512659.1:p.Gly1389LeufsTer7
ENST00000696489.1:c.4154_4164dup	ENSP00000512660.1:p.Gly1389LeufsTer7
ENST00000696490.1:c.4154_4164dup	ENSP00000512661.1:p.Gly1389LeufsTer7
ENST00000282041.11:c.4154_4164dup MANE Select	ENSP00000282041.4:p.Gly1389LeufsTer7
ENST00000282041.9:c.4154_4164dup	ENSP00000282041.4:p.Gly1389LeufsTer7
ENST00000585906.5:n.933_943dup
ENST00000587884.1:c.779_789dup	ENSP00000466990.1:p.Gly264LeufsTer7
ENST00000587974.1:n.4189_4199dup
ENST00000590884.5:c.779_789dup	ENSP00000466403.1:p.Gly264LeufsTer7
ENST00000592272.5:c.779_789dup	ENSP00000467464.1:p.Gly264LeufsTer7
NM_020964.2:c.4154_4164dup	NP_066015.2:p.Gly1389LeufsTer7
XM_011526120.1:c.4181_4191dup	XP_011524422.1:p.Gly1398LeufsTer7
XM_011526121.1:c.4181_4191dup	XP_011524423.1:p.Gly1398LeufsTer7
XM_011526122.1:c.4154_4164dup	XP_011524424.1:p.Gly1389LeufsTer7
XM_011526123.1:c.4181_4191dup	XP_011524425.1:p.Gly1398LeufsTer7
XM_011526124.1:c.4181_4191dup	XP_011524426.1:p.Gly1398LeufsTer7
XM_011526125.1:c.4040_4050dup	XP_011524427.1:p.Gly1351LeufsTer7
XM_011526126.1:c.3116_3126dup	XP_011524428.1:p.Gly1043LeufsTer7
XM_011526127.1:c.4181_4191dup	XP_011524429.1:p.Gly1398LeufsTer7
XM_011526128.1:c.4181_4191dup	XP_011524430.1:p.Gly1398LeufsTer7
XR_935244.1:n.4254_4264dup
NM_020964.3:c.4154_4164dup MANE Select	NP_066015.2:p.Gly1389LeufsTer7
XM_017025889.1:c.4154_4164dup	XP_016881378.1:p.Gly1389LeufsTer7
XM_017025890.2:c.4154_4164dup	XP_016881379.1:p.Gly1389LeufsTer7
XM_017025891.1:c.4013_4023dup	XP_016881380.1:p.Gly1342LeufsTer7
XM_017025892.1:c.3089_3099dup	XP_016881381.1:p.Gly1034LeufsTer7
XM_017025893.1:c.779_789dup	XP_016881382.1:p.Gly264LeufsTer7
XR_001753256.1:n.4236_4246dup
XR_001753257.1:n.4236_4246dup