Canonical Allele Identifier: CA8949446
Gene: EPG5 HGNC NCBI

Linked Data

ClinVar Variation Id: 572684
ClinVar RCV Id: RCV000694125
dbSNP Id: rs762353654

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45930681A>G , CM000680.2:g.45930681A>G GRCh38
NC_000018.9:g.43510647A>G , CM000680.1:g.43510647A>G GRCh37
NC_000018.8:g.41764645A>G NCBI36
NG_042838.1:g.41659T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000587884.2:c.2407T>C ENSP00000466990.2:p.Tyr803His
ENST00000590884.6:c.2407T>C ENSP00000466403.2:p.Tyr803His
ENST00000592272.6:c.2407T>C ENSP00000467464.2:p.Tyr803His
ENST00000696480.1:n.1348T>C
ENST00000696482.1:c.2407T>C ENSP00000512656.1:p.Tyr803His
ENST00000696483.1:c.2407T>C ENSP00000512657.1:p.Tyr803His
ENST00000696484.1:c.2407T>C ENSP00000512658.1:p.Tyr803His
ENST00000696485.1:c.2407T>C ENSP00000512659.1:p.Tyr803His
ENST00000696489.1:c.2407T>C ENSP00000512660.1:p.Tyr803His
ENST00000696490.1:c.2407T>C ENSP00000512661.1:p.Tyr803His
ENST00000282041.11:c.2407T>C MANE Select ENSP00000282041.4:p.Tyr803His
ENST00000282041.9:c.2407T>C ENSP00000282041.4:p.Tyr803His
ENST00000587974.1:n.2442T>C
NM_020964.2:c.2407T>C NP_066015.2:p.Tyr803His
XM_011526120.1:c.2407T>C XP_011524422.1:p.Tyr803His
XM_011526121.1:c.2407T>C XP_011524423.1:p.Tyr803His
XM_011526122.1:c.2407T>C XP_011524424.1:p.Tyr803His
XM_011526123.1:c.2407T>C XP_011524425.1:p.Tyr803His
XM_011526124.1:c.2407T>C XP_011524426.1:p.Tyr803His
XM_011526125.1:c.2407T>C XP_011524427.1:p.Tyr803His
XM_011526126.1:c.1342T>C XP_011524428.1:p.Tyr448His
XM_011526127.1:c.2407T>C XP_011524429.1:p.Tyr803His
XM_011526128.1:c.2407T>C XP_011524430.1:p.Tyr803His
XR_935244.1:n.2507T>C
NM_020964.3:c.2407T>C MANE Select NP_066015.2:p.Tyr803His
XM_017025889.1:c.2407T>C XP_016881378.1:p.Tyr803His
XM_017025890.2:c.2407T>C XP_016881379.1:p.Tyr803His
XM_017025891.1:c.2407T>C XP_016881380.1:p.Tyr803His
XM_017025892.1:c.1342T>C XP_016881381.1:p.Tyr448His
XM_017025893.1:c.-709T>C XP_016881382.1:n.-709T>C
XR_001753256.1:n.2489T>C
XR_001753257.1:n.2489T>C