Canonical Allele Identifier: CA2812342095
Community Standard Title: NM_020964.3(EPG5):c.5305-8C>G
Gene: EPG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45882495G>C , CM000680.2:g.45882495G>C GRCh38
NC_000018.9:g.43462460G>C , CM000680.1:g.43462460G>C GRCh37
NC_000018.8:g.41716458G>C NCBI36
NG_042838.1:g.89845C>G

Transcript Alleles

HGVS Amino-acid Change
NM_020964.3:c.5305-8C>G MANE Select NP_066015.2:n.5305-8C>G
ENST00000282041.11:c.5305-8C>G MANE Select ENSP00000282041.4:n.5305-8C>G
NM_020964.2:c.5305-8C>G NP_066015.2:n.5305-8C>G
ENST00000282041.9:c.5305-8C>G ENSP00000282041.4:n.5305-8C>G
ENST00000585906.5:n.2084-8C>G
ENST00000586655.2:n.3622-64C>G
ENST00000587884.1:c.*1045-8C>G ENSP00000466990.1:n.*1045-8C>G
ENST00000587884.2:c.5431-8C>G ENSP00000466990.2:n.5431-8C>G
ENST00000587973.2:n.1170-8C>G
ENST00000590884.5:c.1930-64C>G ENSP00000466403.1:n.1930-64C>G
ENST00000590884.6:c.5305-64C>G ENSP00000466403.2:n.5305-64C>G
ENST00000592272.5:c.1930-8C>G ENSP00000467464.1:n.1930-8C>G
ENST00000592272.6:c.5305-8C>G ENSP00000467464.2:n.5305-8C>G
ENST00000696481.1:n.1937-8C>G
ENST00000696482.1:c.5045-8C>G ENSP00000512656.1:n.5045-8C>G
ENST00000696483.1:c.5305-8C>G ENSP00000512657.1:n.5305-8C>G
ENST00000696484.1:c.5305-8C>G ENSP00000512658.1:n.5305-8C>G
ENST00000696485.1:c.5305-64C>G ENSP00000512659.1:n.5305-64C>G
ENST00000696489.1:c.5305-8C>G ENSP00000512660.1:n.5305-8C>G
ENST00000696490.1:c.5305-8C>G ENSP00000512661.1:n.5305-8C>G
XM_011526120.1:c.5332-8C>G XP_011524422.1:n.5332-8C>G
XM_011526121.1:c.5332-8C>G XP_011524423.1:n.5332-8C>G
XM_011526122.1:c.5305-8C>G XP_011524424.1:n.5305-8C>G
XM_011526123.1:c.5332-8C>G XP_011524425.1:n.5332-8C>G
XM_011526124.1:c.5332-8C>G XP_011524426.1:n.5332-8C>G
XM_011526125.1:c.5191-8C>G XP_011524427.1:n.5191-8C>G
XM_011526126.1:c.4267-8C>G XP_011524428.1:n.4267-8C>G
XM_011526127.1:c.5332-8C>G XP_011524429.1:n.5332-8C>G
XM_011526128.1:c.5332-64C>G XP_011524430.1:n.5332-64C>G
XM_017025889.1:c.5305-8C>G XP_016881378.1:n.5305-8C>G
XM_017025890.2:c.5305-8C>G XP_016881379.1:n.5305-8C>G
XM_017025891.1:c.5164-8C>G XP_016881380.1:n.5164-8C>G
XM_017025892.1:c.4240-8C>G XP_016881381.1:n.4240-8C>G
XM_017025893.1:c.1930-8C>G XP_016881382.1:n.1930-8C>G
XR_001753256.1:n.5387-8C>G
XR_001753257.1:n.5387-64C>G
XR_935244.1:n.5405-8C>G