Canonical Allele Identifier: CA1694169761
Gene: TOMM7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22816836T= , CM000669.2:g.22816836T= GRCh38
NC_000007.13:g.22856455T= , CM000669.1:g.22856455T= GRCh37
NC_000007.12:g.22822980T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000358435.9:c.152+1164A= MANE Select ENSP00000351214.4:n.152+1164A=
ENST00000358435.8:c.152+1164A= ENSP00000351214.4:n.152+1164A=
ENST00000372879.8:c.289+576A= ENSP00000361970.4:n.289+576A=
ENST00000405021.7:c.140+1164A= ENSP00000385203.3:n.140+1164A=
ENST00000463284.2:n.174-3651A=
ENST00000483581.1:n.336+1164A=
NM_019059.3:c.152+1164A= NP_061932.1:n.152+1164A=
NM_019059.4:c.152+1164A= NP_061932.1:n.152+1164A=
NM_019059.5:c.152+1164A= MANE Select NP_061932.1:n.152+1164A=
NR_168014.1:n.178+1164A=
NR_168015.1:n.130-3651A=
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