Canonical Allele Identifier: CA2321174300
Gene: TIMM44 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7943660A= , CM000681.2:g.7943660A= GRCh38
NC_000019.9:g.8008545A= , CM000681.1:g.8008545A= GRCh37
NC_000019.8:g.7914545A= NCBI36
NG_051180.1:g.5164T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.-9T= MANE Select ENSP00000270538.2:n.-9T=
ENST00000270538.7:c.-9T= ENSP00000270538.2:n.-9T=
ENST00000595876.5:c.-9T= ENSP00000471596.1:n.-9T=
ENST00000600000.1:n.7T=
NM_006351.3:c.-9T= NP_006342.2:n.-9T=
NM_006351.4:c.-9T= MANE Select NP_006342.2:n.-9T=
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