Canonical Allele Identifier: CA394111858

Gene: STUB1 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.731438C>T (hg19) ; chr16:g.681438C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681438C>T , CM000678.2:g.681438C>T	GRCh38
NC_000016.9:g.731438C>T , CM000678.1:g.731438C>T	GRCh37
NC_000016.8:g.671439C>T	NCBI36
NG_034141.1:g.6328C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.359C>T (STUB1) MANE Select	ENSP00000219548.4:p.Ala120Val
ENST00000219548.8:c.359C>T (STUB1)	ENSP00000219548.4:p.Ala120Val
ENST00000563505.5:n.455C>T (STUB1)
ENST00000564370.5:c.143C>T (STUB1)	ENSP00000456875.1:p.Ala48Val
ENST00000565677.5:c.143C>T (STUB1)	ENSP00000457228.1:p.Ala48Val
ENST00000566181.2:n.128C>T (STUB1)
ENST00000566408.5:c.76C>T (STUB1)
ENST00000567173.5:c.302C>T (STUB1)	ENSP00000456591.1:p.Ala101Val
ENST00000569248.5:n.933C>T (STUB1)
ENST00000620831.4:c.-50+38135C>T (MSLN)	ENSP00000482893.1:n.-50+38135C>T
NM_001293197.1:c.143C>T (STUB1)	NP_001280126.1:p.Ala48Val
NM_005861.3:c.359C>T (STUB1)	NP_005852.2:p.Ala120Val
NM_005861.4:c.359C>T (STUB1) MANE Select	NP_005852.2:p.Ala120Val
NM_001293197.2:c.143C>T (STUB1)	NP_001280126.1:p.Ala48Val