Canonical Allele Identifier: CA1694169773
Gene: TOMM7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22816852G= , CM000669.2:g.22816852G= GRCh38
NC_000007.13:g.22856471G= , CM000669.1:g.22856471G= GRCh37
NC_000007.12:g.22822996G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000358435.9:c.152+1148C= MANE Select ENSP00000351214.4:n.152+1148C=
ENST00000358435.8:c.152+1148C= ENSP00000351214.4:n.152+1148C=
ENST00000372879.8:c.289+560C= ENSP00000361970.4:n.289+560C=
ENST00000405021.7:c.140+1148C= ENSP00000385203.3:n.140+1148C=
ENST00000463284.2:n.174-3667C=
ENST00000483581.1:n.336+1148C=
NM_019059.3:c.152+1148C= NP_061932.1:n.152+1148C=
NM_019059.4:c.152+1148C= NP_061932.1:n.152+1148C=
NM_019059.5:c.152+1148C= MANE Select NP_061932.1:n.152+1148C=
NR_168014.1:n.178+1148C=
NR_168015.1:n.130-3667C=
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