Canonical Allele Identifier: CA2321169252
Gene: TIMM44 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7934028G= , CM000681.2:g.7934028G= GRCh38
NC_000019.9:g.7998913G= , CM000681.1:g.7998913G= GRCh37
NC_000019.8:g.7904913G= NCBI36
NG_051180.1:g.14796C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.544-25C= MANE Select ENSP00000270538.2:n.544-25C=
ENST00000270538.7:c.544-25C= ENSP00000270538.2:n.544-25C=
ENST00000595831.5:c.531-25C=
ENST00000595876.5:c.*232-25C= ENSP00000471596.1:n.*232-25C=
ENST00000597926.1:c.448-25C= ENSP00000469389.1:n.448-25C=
ENST00000600748.5:n.529-25C=
NM_006351.3:c.544-25C= NP_006342.2:n.544-25C=
NM_006351.4:c.544-25C= MANE Select NP_006342.2:n.544-25C=
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