Canonical Allele Identifier: CA733133947
Gene: TOMM20 HGNC NCBI

Linked Data

dbSNP Id: rs1468280459
MyVariant Identifiers: chr1:g.235276200_235276202del (hg19) chr1:g.235112885_235112887del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235112887_235112889del , CM000663.2:g.235112887_235112889del GRCh38
NC_000001.10:g.235276202_235276204del , CM000663.1:g.235276202_235276204del GRCh37
NC_000001.9:g.233342825_233342827del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366607.5:c.394-779_394-777del MANE Select ENSP00000355566.4:n.394-779_394-777del
ENST00000366607.4:c.394-779_394-777del ENSP00000355566.4:n.394-779_394-777del
ENST00000467767.5:n.294-779_294-777del
ENST00000473132.1:n.360-779_360-777del
NM_014765.2:c.394-779_394-777del NP_055580.1:n.394-779_394-777del
NM_014765.3:c.394-779_394-777del MANE Select NP_055580.1:n.394-779_394-777del
Search 100 bp 5'
Search 100 bp 3'