Canonical Allele Identifier: CA1228503012
Gene: TOMM20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112881T= , CM000663.2:g.235112881T= GRCh38
NC_000001.10:g.235276196T= , CM000663.1:g.235276196T= GRCh37
NC_000001.9:g.233342819T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366607.5:c.394-773A= MANE Select ENSP00000355566.4:n.394-773A=
ENST00000366607.4:c.394-773A= ENSP00000355566.4:n.394-773A=
ENST00000467767.5:n.294-773A=
ENST00000473132.1:n.360-773A=
NM_014765.2:c.394-773A= NP_055580.1:n.394-773A=
NM_014765.3:c.394-773A= MANE Select NP_055580.1:n.394-773A=