Canonical Allele Identifier: CA1228503013
Gene: TOMM20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112882A= , CM000663.2:g.235112882A= GRCh38
NC_000001.10:g.235276197A= , CM000663.1:g.235276197A= GRCh37
NC_000001.9:g.233342820A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366607.5:c.394-774T= MANE Select ENSP00000355566.4:n.394-774T=
ENST00000366607.4:c.394-774T= ENSP00000355566.4:n.394-774T=
ENST00000467767.5:n.294-774T=
ENST00000473132.1:n.360-774T=
NM_014765.2:c.394-774T= NP_055580.1:n.394-774T=
NM_014765.3:c.394-774T= MANE Select NP_055580.1:n.394-774T=
Search 100 bp 5'
Search 100 bp 3'