Canonical Allele Identifier: CA996242458
Gene: TOMM40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44899826_44899827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000681.2:g.44899826_44899827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000019.9:g.45403083_45403084insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000681.1:g.45403083_45403084insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000019.8:g.50094923_50094924insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_042854.1:g.13607_13608insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000426677.7:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000410339.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000252487.9:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000252487.4:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000405636.6:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000385184.2:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000426677.6:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000410339.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000592041.1:c.160-904_160-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000592434.5:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000466084.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTT...
NM_001128916.1:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001122388.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001128917.1:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001122389.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_006114.2:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_006105.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005258411.2:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005258468.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005258411.4:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005258468.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001128917.2:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_001122389.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_006114.3:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_006105.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001128916.2:c.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001122388.1:n.644-904_644-903insTTTTTTTTTTTTTTTTTTTTTTTTTT...