Canonical Allele Identifier: CA2641627326
Community Standard Title: NM_020964.3(EPG5):c.5305-8_5305-7insG
Gene: EPG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45882494_45882495insC , CM000680.2:g.45882494_45882495insC GRCh38
NC_000018.9:g.43462459_43462460insC , CM000680.1:g.43462459_43462460insC GRCh37
NC_000018.8:g.41716457_41716458insC NCBI36
NG_042838.1:g.89845_89846insG

Transcript Alleles

HGVS Amino-acid Change
NM_020964.3:c.5305-8_5305-7insG MANE Select NP_066015.2:n.5305-8_5305-7insG
ENST00000282041.11:c.5305-8_5305-7insG MANE Select ENSP00000282041.4:n.5305-8_5305-7insG
NM_020964.2:c.5305-8_5305-7insG NP_066015.2:n.5305-8_5305-7insG
ENST00000282041.9:c.5305-8_5305-7insG ENSP00000282041.4:n.5305-8_5305-7insG
ENST00000585906.5:n.2084-8_2084-7insG
ENST00000586655.2:n.3622-64_3622-63insG
ENST00000587884.1:c.*1045-8_*1045-7insG ENSP00000466990.1:n.*1045-8_*1045-7insG
ENST00000587884.2:c.5431-8_5431-7insG ENSP00000466990.2:n.5431-8_5431-7insG
ENST00000587973.2:n.1170-8_1170-7insG
ENST00000590884.5:c.1930-64_1930-63insG ENSP00000466403.1:n.1930-64_1930-63insG
ENST00000590884.6:c.5305-64_5305-63insG ENSP00000466403.2:n.5305-64_5305-63insG
ENST00000592272.5:c.1930-8_1930-7insG ENSP00000467464.1:n.1930-8_1930-7insG
ENST00000592272.6:c.5305-8_5305-7insG ENSP00000467464.2:n.5305-8_5305-7insG
ENST00000696481.1:n.1937-8_1937-7insG
ENST00000696482.1:c.5045-8_5045-7insG ENSP00000512656.1:n.5045-8_5045-7insG
ENST00000696483.1:c.5305-8_5305-7insG ENSP00000512657.1:n.5305-8_5305-7insG
ENST00000696484.1:c.5305-8_5305-7insG ENSP00000512658.1:n.5305-8_5305-7insG
ENST00000696485.1:c.5305-64_5305-63insG ENSP00000512659.1:n.5305-64_5305-63insG
ENST00000696489.1:c.5305-8_5305-7insG ENSP00000512660.1:n.5305-8_5305-7insG
ENST00000696490.1:c.5305-8_5305-7insG ENSP00000512661.1:n.5305-8_5305-7insG
XM_011526120.1:c.5332-8_5332-7insG XP_011524422.1:n.5332-8_5332-7insG
XM_011526121.1:c.5332-8_5332-7insG XP_011524423.1:n.5332-8_5332-7insG
XM_011526122.1:c.5305-8_5305-7insG XP_011524424.1:n.5305-8_5305-7insG
XM_011526123.1:c.5332-8_5332-7insG XP_011524425.1:n.5332-8_5332-7insG
XM_011526124.1:c.5332-8_5332-7insG XP_011524426.1:n.5332-8_5332-7insG
XM_011526125.1:c.5191-8_5191-7insG XP_011524427.1:n.5191-8_5191-7insG
XM_011526126.1:c.4267-8_4267-7insG XP_011524428.1:n.4267-8_4267-7insG
XM_011526127.1:c.5332-8_5332-7insG XP_011524429.1:n.5332-8_5332-7insG
XM_011526128.1:c.5332-64_5332-63insG XP_011524430.1:n.5332-64_5332-63insG
XM_017025889.1:c.5305-8_5305-7insG XP_016881378.1:n.5305-8_5305-7insG
XM_017025890.2:c.5305-8_5305-7insG XP_016881379.1:n.5305-8_5305-7insG
XM_017025891.1:c.5164-8_5164-7insG XP_016881380.1:n.5164-8_5164-7insG
XM_017025892.1:c.4240-8_4240-7insG XP_016881381.1:n.4240-8_4240-7insG
XM_017025893.1:c.1930-8_1930-7insG XP_016881382.1:n.1930-8_1930-7insG
XR_001753256.1:n.5387-8_5387-7insG
XR_001753257.1:n.5387-64_5387-63insG
XR_935244.1:n.5405-8_5405-7insG