Canonical Allele Identifier: CA1694169765
Gene: TOMM7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22816838T= , CM000669.2:g.22816838T= GRCh38
NC_000007.13:g.22856457T= , CM000669.1:g.22856457T= GRCh37
NC_000007.12:g.22822982T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000358435.9:c.152+1162A= MANE Select ENSP00000351214.4:n.152+1162A=
ENST00000358435.8:c.152+1162A= ENSP00000351214.4:n.152+1162A=
ENST00000372879.8:c.289+574A= ENSP00000361970.4:n.289+574A=
ENST00000405021.7:c.140+1162A= ENSP00000385203.3:n.140+1162A=
ENST00000463284.2:n.174-3653A=
ENST00000483581.1:n.336+1162A=
NM_019059.3:c.152+1162A= NP_061932.1:n.152+1162A=
NM_019059.4:c.152+1162A= NP_061932.1:n.152+1162A=
NM_019059.5:c.152+1162A= MANE Select NP_061932.1:n.152+1162A=
NR_168014.1:n.178+1162A=
NR_168015.1:n.130-3653A=
Search 100 bp 5'
Search 100 bp 3'