Canonical Allele Identifier: CA402344767

Gene: EPG5

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45882365C>G , CM000680.2:g.45882365C>G	GRCh38
NC_000018.9:g.43462330C>G , CM000680.1:g.43462330C>G	GRCh37
NC_000018.8:g.41716328C>G	NCBI36
NG_042838.1:g.89975G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020964.3:c.5427G>C MANE Select	NP_066015.2:p.Met1809Ile
ENST00000282041.11:c.5427G>C MANE Select	ENSP00000282041.4:p.Met1809Ile
NM_020964.2:c.5427G>C	NP_066015.2:p.Met1809Ile
ENST00000282041.9:c.5427G>C	ENSP00000282041.4:p.Met1809Ile
ENST00000585906.5:n.2206G>C
ENST00000586655.2:n.3688G>C
ENST00000587884.1:c.*1167G>C	ENSP00000466990.1:n.*1167G>C
ENST00000587884.2:c.5553G>C	ENSP00000466990.2:n.5553G>C
ENST00000587973.2:n.1292G>C
ENST00000590884.5:c.*22G>C	ENSP00000466403.1:n.*22G>C
ENST00000590884.6:c.5371G>C	ENSP00000466403.2:n.5371G>C
ENST00000592272.5:c.2052G>C	ENSP00000467464.1:p.Met684Ile
ENST00000592272.6:c.5427G>C	ENSP00000467464.2:p.Met1809Ile
ENST00000696481.1:n.2059G>C
ENST00000696482.1:c.5167G>C	ENSP00000512656.1:n.5167G>C
ENST00000696483.1:c.5427G>C	ENSP00000512657.1:p.Met1809Ile
ENST00000696484.1:c.5427G>C	ENSP00000512658.1:p.Met1809Ile
ENST00000696485.1:c.*22G>C	ENSP00000512659.1:n.*22G>C
ENST00000696489.1:c.5427G>C	ENSP00000512660.1:p.Met1809Ile
ENST00000696490.1:c.5427G>C	ENSP00000512661.1:p.Met1809Ile
XM_011526120.1:c.5454G>C	XP_011524422.1:p.Met1818Ile
XM_011526121.1:c.5454G>C	XP_011524423.1:p.Met1818Ile
XM_011526122.1:c.5427G>C	XP_011524424.1:p.Met1809Ile
XM_011526123.1:c.5454G>C	XP_011524425.1:p.Met1818Ile
XM_011526124.1:c.5454G>C	XP_011524426.1:p.Met1818Ile
XM_011526125.1:c.5313G>C	XP_011524427.1:p.Met1771Ile
XM_011526126.1:c.4389G>C	XP_011524428.1:p.Met1463Ile
XM_011526127.1:c.5454G>C	XP_011524429.1:p.Met1818Ile
XM_011526128.1:c.*22G>C	XP_011524430.1:n.*22G>C
XM_017025889.1:c.5427G>C	XP_016881378.1:p.Met1809Ile
XM_017025890.2:c.5427G>C	XP_016881379.1:p.Met1809Ile
XM_017025891.1:c.5286G>C	XP_016881380.1:p.Met1762Ile
XM_017025892.1:c.4362G>C	XP_016881381.1:p.Met1454Ile
XM_017025893.1:c.2052G>C	XP_016881382.1:p.Met684Ile
XR_001753256.1:n.5509G>C
XR_001753257.1:n.5453G>C
XR_935244.1:n.5527G>C