Canonical Allele Identifier: CA882653582

Gene: TOMM40

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44893408G>A , CM000681.2:g.44893408G>A	GRCh38
NC_000019.9:g.45396665G>A , CM000681.1:g.45396665G>A	GRCh37
NC_000019.8:g.50088505G>A	NCBI36
NG_042854.1:g.7189G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426677.7:c.436-372G>A MANE Select	ENSP00000410339.1:n.436-372G>A
ENST00000252487.9:c.436-372G>A	ENSP00000252487.4:n.436-372G>A
ENST00000405636.6:c.436-372G>A	ENSP00000385184.2:n.436-372G>A
ENST00000426677.6:c.436-372G>A	ENSP00000410339.1:n.436-372G>A
ENST00000589649.1:c.436-372G>A	ENSP00000465032.1:n.436-372G>A
ENST00000592434.5:c.436-372G>A	ENSP00000466084.1:n.436-372G>A
NM_001128916.1:c.436-372G>A	NP_001122388.1:n.436-372G>A
NM_001128917.1:c.436-372G>A	NP_001122389.1:n.436-372G>A
NM_006114.2:c.436-372G>A	NP_006105.1:n.436-372G>A
XM_005258411.2:c.436-372G>A	XP_005258468.1:n.436-372G>A
XM_005258411.4:c.436-372G>A	XP_005258468.1:n.436-372G>A
NM_001128917.2:c.436-372G>A MANE Select	NP_001122389.1:n.436-372G>A
NM_006114.3:c.436-372G>A	NP_006105.1:n.436-372G>A
NM_001128916.2:c.436-372G>A	NP_001122388.1:n.436-372G>A