Canonical Allele Identifier: CA2585710475

Gene: TOMM40

Linked Data

• gnomAD v4: 19-44892353-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44892357del , CM000681.2:g.44892357del	GRCh38
NC_000019.9:g.45395614del , CM000681.1:g.45395614del	GRCh37
NC_000019.8:g.50087454del	NCBI36
NG_042854.1:g.6138del

Transcript Alleles

HGVS	Amino-acid change
ENST00000426677.7:c.275-36del MANE Select	ENSP00000410339.1:n.275-36del
ENST00000252487.9:c.275-36del	ENSP00000252487.4:n.275-36del
ENST00000405636.6:c.275-36del	ENSP00000385184.2:n.275-36del
ENST00000426677.6:c.275-36del	ENSP00000410339.1:n.275-36del
ENST00000589649.1:c.275-36del	ENSP00000465032.1:n.275-36del
ENST00000592434.5:c.275-36del	ENSP00000466084.1:n.275-36del
NM_001128916.1:c.275-36del	NP_001122388.1:n.275-36del
NM_001128917.1:c.275-36del	NP_001122389.1:n.275-36del
NM_006114.2:c.275-36del	NP_006105.1:n.275-36del
XM_005258411.2:c.275-36del	XP_005258468.1:n.275-36del
XM_005258411.4:c.275-36del	XP_005258468.1:n.275-36del
NM_001128917.2:c.275-36del MANE Select	NP_001122389.1:n.275-36del
NM_006114.3:c.275-36del	NP_006105.1:n.275-36del
NM_001128916.2:c.275-36del	NP_001122388.1:n.275-36del