Canonical Allele Identifier: CA2641629188

Gene: EPG5

Linked Data

• gnomAD v4: 18-45910533-T-TTAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45910534_45910535insAAAAAAT , CM000680.2:g.45910534_45910535insAAAAAAT	GRCh38
NC_000018.9:g.43490499_43490500insAAAAAAT , CM000680.1:g.43490499_43490500insAAAAAAT	GRCh37
NC_000018.8:g.41744497_41744498insAAAAAAT	NCBI36
NG_042838.1:g.61806_61807insTTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586655.2:n.2376_2377insTTTTTTA
ENST00000587884.2:c.4192_4193insTTTTTTA	ENSP00000466990.2:p.Lys1398IlefsTer3
ENST00000590884.6:c.4192_4193insTTTTTTA	ENSP00000466403.2:p.Lys1398IlefsTer3
ENST00000592272.6:c.4192_4193insTTTTTTA	ENSP00000467464.2:p.Lys1398IlefsTer3
ENST00000696482.1:c.3932_3933insTTTTTTA	ENSP00000512656.1:n.3932_3933insTTTTTTA
ENST00000696483.1:c.4192_4193insTTTTTTA	ENSP00000512657.1:p.Lys1398IlefsTer3
ENST00000696484.1:c.4192_4193insTTTTTTA	ENSP00000512658.1:p.Lys1398IlefsTer3
ENST00000696485.1:c.4192_4193insTTTTTTA	ENSP00000512659.1:p.Lys1398IlefsTer3
ENST00000696489.1:c.4192_4193insTTTTTTA	ENSP00000512660.1:p.Lys1398IlefsTer3
ENST00000696490.1:c.4192_4193insTTTTTTA	ENSP00000512661.1:p.Lys1398IlefsTer3
ENST00000282041.11:c.4192_4193insTTTTTTA MANE Select	ENSP00000282041.4:p.Lys1398IlefsTer3
ENST00000282041.9:c.4192_4193insTTTTTTA	ENSP00000282041.4:p.Lys1398IlefsTer3
ENST00000585906.5:n.971_972insTTTTTTA
ENST00000587884.1:c.817_818insTTTTTTA	ENSP00000466990.1:p.Lys273IlefsTer3
ENST00000587974.1:n.4227_4228insTTTTTTA
ENST00000590884.5:c.817_818insTTTTTTA	ENSP00000466403.1:p.Lys273IlefsTer3
ENST00000592272.5:c.817_818insTTTTTTA	ENSP00000467464.1:p.Lys273IlefsTer3
NM_020964.2:c.4192_4193insTTTTTTA	NP_066015.2:p.Lys1398IlefsTer3
XM_011526120.1:c.4219_4220insTTTTTTA	XP_011524422.1:p.Lys1407IlefsTer3
XM_011526121.1:c.4219_4220insTTTTTTA	XP_011524423.1:p.Lys1407IlefsTer3
XM_011526122.1:c.4192_4193insTTTTTTA	XP_011524424.1:p.Lys1398IlefsTer3
XM_011526123.1:c.4219_4220insTTTTTTA	XP_011524425.1:p.Lys1407IlefsTer3
XM_011526124.1:c.4219_4220insTTTTTTA	XP_011524426.1:p.Lys1407IlefsTer3
XM_011526125.1:c.4078_4079insTTTTTTA	XP_011524427.1:p.Lys1360IlefsTer3
XM_011526126.1:c.3154_3155insTTTTTTA	XP_011524428.1:p.Lys1052IlefsTer3
XM_011526127.1:c.4219_4220insTTTTTTA	XP_011524429.1:p.Lys1407IlefsTer3
XM_011526128.1:c.4219_4220insTTTTTTA	XP_011524430.1:p.Lys1407IlefsTer3
XR_935244.1:n.4292_4293insTTTTTTA
NM_020964.3:c.4192_4193insTTTTTTA MANE Select	NP_066015.2:p.Lys1398IlefsTer3
XM_017025889.1:c.4192_4193insTTTTTTA	XP_016881378.1:p.Lys1398IlefsTer3
XM_017025890.2:c.4192_4193insTTTTTTA	XP_016881379.1:p.Lys1398IlefsTer3
XM_017025891.1:c.4051_4052insTTTTTTA	XP_016881380.1:p.Lys1351IlefsTer3
XM_017025892.1:c.3127_3128insTTTTTTA	XP_016881381.1:p.Lys1043IlefsTer3
XM_017025893.1:c.817_818insTTTTTTA	XP_016881382.1:p.Lys273IlefsTer3
XR_001753256.1:n.4274_4275insTTTTTTA
XR_001753257.1:n.4274_4275insTTTTTTA