Canonical Allele Identifier: CA2588035132
Gene: TIMM44 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7934006_7934018del , CM000681.2:g.7934006_7934018del GRCh38
NC_000019.9:g.7998891_7998903del , CM000681.1:g.7998891_7998903del GRCh37
NC_000019.8:g.7904891_7904903del NCBI36
NG_051180.1:g.14806_14818del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.544-15_544-3del MANE Select ENSP00000270538.2:n.544-15_544-3del
ENST00000270538.7:c.544-15_544-3del ENSP00000270538.2:n.544-15_544-3del
ENST00000595831.5:c.531-15_531-3del
ENST00000595876.5:c.*232-15_*232-3del ENSP00000471596.1:n.*232-15_*232-3del
ENST00000597926.1:c.448-15_448-3del ENSP00000469389.1:n.448-15_448-3del
ENST00000600748.5:n.529-15_529-3del
NM_006351.3:c.544-15_544-3del NP_006342.2:n.544-15_544-3del
NM_006351.4:c.544-15_544-3del MANE Select NP_006342.2:n.544-15_544-3del