Canonical Allele Identifier: CA2641631658

Gene: EPG5

Linked Data

• gnomAD v4: 18-45930868-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45930868_45930869insT , CM000680.2:g.45930868_45930869insT	GRCh38
NC_000018.9:g.43510834_43510835insT , CM000680.1:g.43510834_43510835insT	GRCh37
NC_000018.8:g.41764832_41764833insT	NCBI36
NG_042838.1:g.41471_41472insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587884.2:c.2258-39_2258-38insA	ENSP00000466990.2:n.2258-39_2258-38insA
ENST00000590884.6:c.2258-39_2258-38insA	ENSP00000466403.2:n.2258-39_2258-38insA
ENST00000592272.6:c.2258-39_2258-38insA	ENSP00000467464.2:n.2258-39_2258-38insA
ENST00000696480.1:n.1199-39_1199-38insA
ENST00000696482.1:c.2258-39_2258-38insA	ENSP00000512656.1:n.2258-39_2258-38insA
ENST00000696483.1:c.2258-39_2258-38insA	ENSP00000512657.1:n.2258-39_2258-38insA
ENST00000696484.1:c.2258-39_2258-38insA	ENSP00000512658.1:n.2258-39_2258-38insA
ENST00000696485.1:c.2258-39_2258-38insA	ENSP00000512659.1:n.2258-39_2258-38insA
ENST00000696489.1:c.2258-39_2258-38insA	ENSP00000512660.1:n.2258-39_2258-38insA
ENST00000696490.1:c.2258-39_2258-38insA	ENSP00000512661.1:n.2258-39_2258-38insA
ENST00000282041.11:c.2258-39_2258-38insA MANE Select	ENSP00000282041.4:n.2258-39_2258-38insA
ENST00000282041.9:c.2258-39_2258-38insA	ENSP00000282041.4:n.2258-39_2258-38insA
ENST00000587974.1:n.2293-39_2293-38insA
NM_020964.2:c.2258-39_2258-38insA	NP_066015.2:n.2258-39_2258-38insA
XM_011526120.1:c.2258-39_2258-38insA	XP_011524422.1:n.2258-39_2258-38insA
XM_011526121.1:c.2258-39_2258-38insA	XP_011524423.1:n.2258-39_2258-38insA
XM_011526122.1:c.2258-39_2258-38insA	XP_011524424.1:n.2258-39_2258-38insA
XM_011526123.1:c.2258-39_2258-38insA	XP_011524425.1:n.2258-39_2258-38insA
XM_011526124.1:c.2258-39_2258-38insA	XP_011524426.1:n.2258-39_2258-38insA
XM_011526125.1:c.2258-39_2258-38insA	XP_011524427.1:n.2258-39_2258-38insA
XM_011526126.1:c.1193-39_1193-38insA	XP_011524428.1:n.1193-39_1193-38insA
XM_011526127.1:c.2258-39_2258-38insA	XP_011524429.1:n.2258-39_2258-38insA
XM_011526128.1:c.2258-39_2258-38insA	XP_011524430.1:n.2258-39_2258-38insA
XR_935244.1:n.2358-39_2358-38insA
NM_020964.3:c.2258-39_2258-38insA MANE Select	NP_066015.2:n.2258-39_2258-38insA
XM_017025889.1:c.2258-39_2258-38insA	XP_016881378.1:n.2258-39_2258-38insA
XM_017025890.2:c.2258-39_2258-38insA	XP_016881379.1:n.2258-39_2258-38insA
XM_017025891.1:c.2258-39_2258-38insA	XP_016881380.1:n.2258-39_2258-38insA
XM_017025892.1:c.1193-39_1193-38insA	XP_016881381.1:n.1193-39_1193-38insA
XM_017025893.1:c.-858-39_-858-38insA	XP_016881382.1:n.-858-39_-858-38insA
XR_001753256.1:n.2340-39_2340-38insA
XR_001753257.1:n.2340-39_2340-38insA