Canonical Allele Identifier: CA1228503010
Gene: TOMM20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112878A= , CM000663.2:g.235112878A= GRCh38
NC_000001.10:g.235276193A= , CM000663.1:g.235276193A= GRCh37
NC_000001.9:g.233342816A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366607.5:c.394-770T= MANE Select ENSP00000355566.4:n.394-770T=
ENST00000366607.4:c.394-770T= ENSP00000355566.4:n.394-770T=
ENST00000467767.5:n.294-770T=
ENST00000473132.1:n.360-770T=
NM_014765.2:c.394-770T= NP_055580.1:n.394-770T=
NM_014765.3:c.394-770T= MANE Select NP_055580.1:n.394-770T=