Canonical Allele Identifier: CA2588035143
Gene: TIMM44 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7934043del , CM000681.2:g.7934043del GRCh38
NC_000019.9:g.7998928del , CM000681.1:g.7998928del GRCh37
NC_000019.8:g.7904928del NCBI36
NG_051180.1:g.14783del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.544-38del MANE Select ENSP00000270538.2:n.544-38del
ENST00000270538.7:c.544-38del ENSP00000270538.2:n.544-38del
ENST00000595831.5:c.531-38del
ENST00000595876.5:c.*232-38del ENSP00000471596.1:n.*232-38del
ENST00000597926.1:c.448-38del ENSP00000469389.1:n.448-38del
ENST00000600748.5:n.529-38del
NM_006351.3:c.544-38del NP_006342.2:n.544-38del
NM_006351.4:c.544-38del MANE Select NP_006342.2:n.544-38del