Canonical Allele Identifier: CA493008456

Gene: STUB1 MSLN

Linked Data

• COSMIC: COSM5514439
• MyVariant Identifiers: chr16:g.731505G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681505G>T , CM000678.2:g.681505G>T	GRCh38
NC_000016.9:g.731505G>T , CM000678.1:g.731505G>T	GRCh37
NC_000016.8:g.671506G>T	NCBI36
NG_034141.1:g.6395G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.426G>T (STUB1) MANE Select	ENSP00000219548.4:p.Ala142=
ENST00000219548.8:c.426G>T (STUB1)	ENSP00000219548.4:p.Ala142=
ENST00000563505.5:n.522G>T (STUB1)
ENST00000564316.1:c.25G>T (STUB1)
ENST00000564370.5:c.210G>T (STUB1)	ENSP00000456875.1:p.Ala70=
ENST00000565677.5:c.210G>T (STUB1)	ENSP00000457228.1:p.Ala70=
ENST00000566181.2:n.195G>T (STUB1)
ENST00000566408.5:c.143G>T (STUB1)
ENST00000567173.5:c.369G>T (STUB1)	ENSP00000456591.1:p.Ala123=
ENST00000569248.5:n.1000G>T (STUB1)
ENST00000620831.4:c.-50+38202G>T (MSLN)	ENSP00000482893.1:n.-50+38202G>T
NM_001293197.1:c.210G>T (STUB1)	NP_001280126.1:p.Ala70=
NM_005861.3:c.426G>T (STUB1)	NP_005852.2:p.Ala142=
NM_005861.4:c.426G>T (STUB1) MANE Select	NP_005852.2:p.Ala142=
NM_001293197.2:c.210G>T (STUB1)	NP_001280126.1:p.Ala70=