Canonical Allele Identifier: CA2321169222
Gene: TIMM44 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7933973C= , CM000681.2:g.7933973C= GRCh38
NC_000019.9:g.7998858C= , CM000681.1:g.7998858C= GRCh37
NC_000019.8:g.7904858C= NCBI36
NG_051180.1:g.14851G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.574G= MANE Select ENSP00000270538.2:p.Asp192=
ENST00000270538.7:c.574G= ENSP00000270538.2:p.Asp192=
ENST00000595831.5:c.561G=
ENST00000595876.5:c.*262G= ENSP00000471596.1:n.*262G=
ENST00000597926.1:c.478G= ENSP00000469389.1:p.Asp160=
ENST00000600748.5:n.559G=
NM_006351.3:c.574G= NP_006342.2:p.Asp192=
NM_006351.4:c.574G= MANE Select NP_006342.2:p.Asp192=