Canonical Allele Identifier: CA2321169255
Gene: TIMM44 HGNC NCBI

Linked Data

dbSNP Id: rs755896129
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7934031G>T , CM000681.2:g.7934031G>T GRCh38
NC_000019.9:g.7998916G>T , CM000681.1:g.7998916G>T GRCh37
NC_000019.8:g.7904916G>T NCBI36
NG_051180.1:g.14793C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.544-28C>A MANE Select ENSP00000270538.2:n.544-28C>A
ENST00000270538.7:c.544-28C>A ENSP00000270538.2:n.544-28C>A
ENST00000595831.5:c.531-28C>A
ENST00000595876.5:c.*232-28C>A ENSP00000471596.1:n.*232-28C>A
ENST00000597926.1:c.448-28C>A ENSP00000469389.1:n.448-28C>A
ENST00000600748.5:n.529-28C>A
NM_006351.3:c.544-28C>A NP_006342.2:n.544-28C>A
NM_006351.4:c.544-28C>A MANE Select NP_006342.2:n.544-28C>A
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