Canonical Allele Identifier: CA402340232
Gene: EPG5 HGNC NCBI

Linked Data

dbSNP Id: rs2049872647

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45910698G>A , CM000680.2:g.45910698G>A GRCh38
NC_000018.9:g.43490663G>A , CM000680.1:g.43490663G>A GRCh37
NC_000018.8:g.41744661G>A NCBI36
NG_042838.1:g.61642C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000586655.2:n.2212C>T
ENST00000587884.2:c.4028C>T ENSP00000466990.2:p.Pro1343Leu
ENST00000590884.6:c.4028C>T ENSP00000466403.2:p.Pro1343Leu
ENST00000592272.6:c.4028C>T ENSP00000467464.2:p.Pro1343Leu
ENST00000696482.1:c.3768C>T ENSP00000512656.1:n.3768C>T
ENST00000696483.1:c.4028C>T ENSP00000512657.1:p.Pro1343Leu
ENST00000696484.1:c.4028C>T ENSP00000512658.1:p.Pro1343Leu
ENST00000696485.1:c.4028C>T ENSP00000512659.1:p.Pro1343Leu
ENST00000696489.1:c.4028C>T ENSP00000512660.1:p.Pro1343Leu
ENST00000696490.1:c.4028C>T ENSP00000512661.1:p.Pro1343Leu
ENST00000282041.11:c.4028C>T MANE Select ENSP00000282041.4:p.Pro1343Leu
ENST00000282041.9:c.4028C>T ENSP00000282041.4:p.Pro1343Leu
ENST00000585906.5:n.807C>T
ENST00000587884.1:c.653C>T ENSP00000466990.1:p.Pro218Leu
ENST00000587974.1:n.4063C>T
ENST00000590884.5:c.653C>T ENSP00000466403.1:p.Pro218Leu
ENST00000592272.5:c.653C>T ENSP00000467464.1:p.Pro218Leu
NM_020964.2:c.4028C>T NP_066015.2:p.Pro1343Leu
XM_011526120.1:c.4055C>T XP_011524422.1:p.Pro1352Leu
XM_011526121.1:c.4055C>T XP_011524423.1:p.Pro1352Leu
XM_011526122.1:c.4028C>T XP_011524424.1:p.Pro1343Leu
XM_011526123.1:c.4055C>T XP_011524425.1:p.Pro1352Leu
XM_011526124.1:c.4055C>T XP_011524426.1:p.Pro1352Leu
XM_011526125.1:c.3914C>T XP_011524427.1:p.Pro1305Leu
XM_011526126.1:c.2990C>T XP_011524428.1:p.Pro997Leu
XM_011526127.1:c.4055C>T XP_011524429.1:p.Pro1352Leu
XM_011526128.1:c.4055C>T XP_011524430.1:p.Pro1352Leu
XR_935244.1:n.4128C>T
NM_020964.3:c.4028C>T MANE Select NP_066015.2:p.Pro1343Leu
XM_017025889.1:c.4028C>T XP_016881378.1:p.Pro1343Leu
XM_017025890.2:c.4028C>T XP_016881379.1:p.Pro1343Leu
XM_017025891.1:c.3887C>T XP_016881380.1:p.Pro1296Leu
XM_017025892.1:c.2963C>T XP_016881381.1:p.Pro988Leu
XM_017025893.1:c.653C>T XP_016881382.1:p.Pro218Leu
XR_001753256.1:n.4110C>T
XR_001753257.1:n.4110C>T