Canonical Allele Identifier: CA2201204457

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681424C= , CM000678.2:g.681424C= GRCh38
NC_000016.9:g.731424C= , CM000678.1:g.731424C= GRCh37
NC_000016.8:g.671425C= NCBI36
NG_034141.1:g.6314C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.359-14C= (STUB1) MANE Select ENSP00000219548.4:n.359-14C=
ENST00000219548.8:c.359-14C= (STUB1) ENSP00000219548.4:n.359-14C=
ENST00000563505.5:n.455-14C= (STUB1)
ENST00000564370.5:c.143-14C= (STUB1) ENSP00000456875.1:n.143-14C=
ENST00000565677.5:c.143-14C= (STUB1) ENSP00000457228.1:n.143-14C=
ENST00000566181.2:n.128-14C= (STUB1)
ENST00000566408.5:c.76-14C= (STUB1)
ENST00000567173.5:c.302-14C= (STUB1) ENSP00000456591.1:n.302-14C=
ENST00000569248.5:n.933-14C= (STUB1)
ENST00000620831.4:c.-50+38121C= (MSLN) ENSP00000482893.1:n.-50+38121C=
NM_001293197.1:c.143-14C= (STUB1) NP_001280126.1:n.143-14C=
NM_005861.3:c.359-14C= (STUB1) NP_005852.2:n.359-14C=
NM_005861.4:c.359-14C= (STUB1) MANE Select NP_005852.2:n.359-14C=
NM_001293197.2:c.143-14C= (STUB1) NP_001280126.1:n.143-14C=