Canonical Allele Identifier: CA1228503017

Gene: TOMM20

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235112884_235112887delinsAACC , CM000663.2:g.235112884_235112887delinsAACC	GRCh38
NC_000001.10:g.235276199_235276202delinsAACC , CM000663.1:g.235276199_235276202delinsAACC	GRCh37
NC_000001.9:g.233342822_233342825delinsAACC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366607.5:c.394-779_394-776delinsGGTT MANE Select	ENSP00000355566.4:n.394-779_394-776delinsGGTT
ENST00000366607.4:c.394-779_394-776delinsGGTT	ENSP00000355566.4:n.394-779_394-776delinsGGTT
ENST00000467767.5:n.294-779_294-776delinsGGTT
ENST00000473132.1:n.360-779_360-776delinsGGTT
NM_014765.2:c.394-779_394-776delinsGGTT	NP_055580.1:n.394-779_394-776delinsGGTT
NM_014765.3:c.394-779_394-776delinsGGTT MANE Select	NP_055580.1:n.394-779_394-776delinsGGTT