Canonical Allele Identifier: CA2841903492
Gene: TIMM44 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7943516dup , CM000681.2:g.7943516dup GRCh38
NC_000019.9:g.8008401dup , CM000681.1:g.8008401dup GRCh37
NC_000019.8:g.7914401dup NCBI36
NG_051180.1:g.5308dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.45+91dup MANE Select ENSP00000270538.2:n.45+91dup
ENST00000270538.7:c.45+91dup ENSP00000270538.2:n.45+91dup
ENST00000595831.5:c.29+91dup
ENST00000595876.5:c.45+91dup ENSP00000471596.1:n.45+91dup
ENST00000597926.1:c.45+91dup ENSP00000469389.1:n.45+91dup
ENST00000600000.1:n.60+91dup
ENST00000600748.5:n.30+91dup
NM_006351.3:c.45+91dup NP_006342.2:n.45+91dup
NM_006351.4:c.45+91dup MANE Select NP_006342.2:n.45+91dup
Search 100 bp 5'
Search 100 bp 3'