Canonical Allele Identifier: CA2630854887

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681657_681660dup , CM000678.2:g.681657_681660dup GRCh38
NC_000016.9:g.731657_731660dup , CM000678.1:g.731657_731660dup GRCh37
NC_000016.8:g.671658_671661dup NCBI36
NG_034141.1:g.6547_6550dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.524+54_524+57dup (STUB1) MANE Select ENSP00000219548.4:n.524+54_524+57dup
ENST00000219548.8:c.524+54_524+57dup (STUB1) ENSP00000219548.4:n.524+54_524+57dup
ENST00000563505.5:n.620+54_620+57dup (STUB1)
ENST00000564316.1:c.123+54_123+57dup (STUB1)
ENST00000564370.5:c.308+54_308+57dup (STUB1) ENSP00000456875.1:n.308+54_308+57dup
ENST00000565677.5:c.308+54_308+57dup (STUB1) ENSP00000457228.1:n.308+54_308+57dup
ENST00000566181.2:n.293+54_293+57dup (STUB1)
ENST00000566408.5:c.241+54_241+57dup (STUB1)
ENST00000567173.5:c.467+54_467+57dup (STUB1) ENSP00000456591.1:n.467+54_467+57dup
ENST00000569248.5:n.1098+54_1098+57dup (STUB1)
ENST00000620831.4:c.-50+38354_-50+38357dup (MSLN) ENSP00000482893.1:n.-50+38354_-50+38357dup
NM_001293197.1:c.308+54_308+57dup (STUB1) NP_001280126.1:n.308+54_308+57dup
NM_005861.3:c.524+54_524+57dup (STUB1) NP_005852.2:n.524+54_524+57dup
NM_005861.4:c.524+54_524+57dup (STUB1) MANE Select NP_005852.2:n.524+54_524+57dup
NM_001293197.2:c.308+54_308+57dup (STUB1) NP_001280126.1:n.308+54_308+57dup