Canonical Allele Identifier: CA882657783
Gene: TOMM40 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44899825_44899826del , CM000681.2:g.44899825_44899826del GRCh38
NC_000019.9:g.45403082_45403083del , CM000681.1:g.45403082_45403083del GRCh37
NC_000019.8:g.50094922_50094923del NCBI36
NG_042854.1:g.13606_13607del

Transcript Alleles

HGVS Amino-acid Change
ENST00000426677.7:c.644-905_644-904del MANE Select ENSP00000410339.1:n.644-905_644-904del
ENST00000252487.9:c.644-905_644-904del ENSP00000252487.4:n.644-905_644-904del
ENST00000405636.6:c.644-905_644-904del ENSP00000385184.2:n.644-905_644-904del
ENST00000426677.6:c.644-905_644-904del ENSP00000410339.1:n.644-905_644-904del
ENST00000592041.1:c.160-905_160-904del
ENST00000592434.5:c.644-905_644-904del ENSP00000466084.1:n.644-905_644-904del
NM_001128916.1:c.644-905_644-904del NP_001122388.1:n.644-905_644-904del
NM_001128917.1:c.644-905_644-904del NP_001122389.1:n.644-905_644-904del
NM_006114.2:c.644-905_644-904del NP_006105.1:n.644-905_644-904del
XM_005258411.2:c.644-905_644-904del XP_005258468.1:n.644-905_644-904del
XM_005258411.4:c.644-905_644-904del XP_005258468.1:n.644-905_644-904del
NM_001128917.2:c.644-905_644-904del MANE Select NP_001122389.1:n.644-905_644-904del
NM_006114.3:c.644-905_644-904del NP_006105.1:n.644-905_644-904del
NM_001128916.2:c.644-905_644-904del NP_001122388.1:n.644-905_644-904del
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