Canonical Allele Identifier: CA2588036425
Gene: TIMM44 HGNC NCBI

Linked Data

gnomAD v4: 19-7943524-C-CA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7943526dup , CM000681.2:g.7943526dup GRCh38
NC_000019.9:g.8008411dup , CM000681.1:g.8008411dup GRCh37
NC_000019.8:g.7914411dup NCBI36
NG_051180.1:g.5299dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.45+82dup MANE Select ENSP00000270538.2:n.45+82dup
ENST00000270538.7:c.45+82dup ENSP00000270538.2:n.45+82dup
ENST00000595831.5:c.29+82dup
ENST00000595876.5:c.45+82dup ENSP00000471596.1:n.45+82dup
ENST00000597926.1:c.45+82dup ENSP00000469389.1:n.45+82dup
ENST00000600000.1:n.60+82dup
ENST00000600748.5:n.30+82dup
NM_006351.3:c.45+82dup NP_006342.2:n.45+82dup
NM_006351.4:c.45+82dup MANE Select NP_006342.2:n.45+82dup
Search 100 bp 5'
Search 100 bp 3'