Canonical Allele Identifier: CA996250885
Gene: TOMM40 HGNC NCBI

Linked Data

dbSNP Id: rs1969477363

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44892067A>G , CM000681.2:g.44892067A>G GRCh38
NC_000019.9:g.45395324A>G , CM000681.1:g.45395324A>G GRCh37
NC_000019.8:g.50087164A>G NCBI36
NG_042854.1:g.5848A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426677.7:c.275-326A>G MANE Select ENSP00000410339.1:n.275-326A>G
ENST00000252487.9:c.275-326A>G ENSP00000252487.4:n.275-326A>G
ENST00000405636.6:c.275-326A>G ENSP00000385184.2:n.275-326A>G
ENST00000426677.6:c.275-326A>G ENSP00000410339.1:n.275-326A>G
ENST00000589649.1:c.275-326A>G ENSP00000465032.1:n.275-326A>G
ENST00000592434.5:c.275-326A>G ENSP00000466084.1:n.275-326A>G
NM_001128916.1:c.275-326A>G NP_001122388.1:n.275-326A>G
NM_001128917.1:c.275-326A>G NP_001122389.1:n.275-326A>G
NM_006114.2:c.275-326A>G NP_006105.1:n.275-326A>G
XM_005258411.2:c.275-326A>G XP_005258468.1:n.275-326A>G
XM_005258411.4:c.275-326A>G XP_005258468.1:n.275-326A>G
NM_001128917.2:c.275-326A>G MANE Select NP_001122389.1:n.275-326A>G
NM_006114.3:c.275-326A>G NP_006105.1:n.275-326A>G
NM_001128916.2:c.275-326A>G NP_001122388.1:n.275-326A>G