Canonical Allele Identifier: CA2338163797

Gene: TOMM40

Linked Data

• dbSNP Id: rs741780

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44901174T>G , CM000681.2:g.44901174T>G	GRCh38
NC_000019.9:g.45404431T>G , CM000681.1:g.45404431T>G	GRCh37
NC_000019.8:g.50096271T>G	NCBI36
NG_007084.2:g.393T>G
NG_042854.1:g.14955T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000426677.7:c.844-34T>G MANE Select	ENSP00000410339.1:n.844-34T>G
ENST00000252487.9:c.844-34T>G	ENSP00000252487.4:n.844-34T>G
ENST00000405636.6:c.844-34T>G	ENSP00000385184.2:n.844-34T>G
ENST00000426677.6:c.844-34T>G	ENSP00000410339.1:n.844-34T>G
ENST00000592041.1:c.360-34T>G
ENST00000592434.5:c.844-34T>G	ENSP00000466084.1:n.844-34T>G
NM_001128916.1:c.844-34T>G	NP_001122388.1:n.844-34T>G
NM_001128917.1:c.844-34T>G	NP_001122389.1:n.844-34T>G
NM_006114.2:c.844-34T>G	NP_006105.1:n.844-34T>G
XM_005258411.2:c.844-34T>G	XP_005258468.1:n.844-34T>G
XM_005258411.4:c.844-34T>G	XP_005258468.1:n.844-34T>G
NM_001128917.2:c.844-34T>G MANE Select	NP_001122389.1:n.844-34T>G
NM_006114.3:c.844-34T>G	NP_006105.1:n.844-34T>G
NM_001128916.2:c.844-34T>G	NP_001122388.1:n.844-34T>G