Canonical Allele Identifier: CA394111387

Gene: STUB1 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.731288T>A (hg19) ; chr16:g.681288T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681288T>A , CM000678.2:g.681288T>A	GRCh38
NC_000016.9:g.731288T>A , CM000678.1:g.731288T>A	GRCh37
NC_000016.8:g.671289T>A	NCBI36
NG_034141.1:g.6178T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.296T>A (STUB1) MANE Select	ENSP00000219548.4:p.Phe99Tyr
ENST00000219548.8:c.296T>A (STUB1)	ENSP00000219548.4:p.Phe99Tyr
ENST00000563505.5:n.392T>A (STUB1)
ENST00000564370.5:c.80T>A (STUB1)	ENSP00000456875.1:p.Phe27Tyr
ENST00000565677.5:c.80T>A (STUB1)	ENSP00000457228.1:p.Phe27Tyr
ENST00000566181.2:n.65T>A (STUB1)
ENST00000566408.5:c.13T>A (STUB1)
ENST00000567173.5:c.239T>A (STUB1)	ENSP00000456591.1:p.Phe80Tyr
ENST00000567790.1:n.326T>A (STUB1)
ENST00000569248.5:n.870T>A (STUB1)
ENST00000620831.4:c.-50+37985T>A (MSLN)	ENSP00000482893.1:n.-50+37985T>A
NM_001293197.1:c.80T>A (STUB1)	NP_001280126.1:p.Phe27Tyr
NM_005861.3:c.296T>A (STUB1)	NP_005852.2:p.Phe99Tyr
NM_005861.4:c.296T>A (STUB1) MANE Select	NP_005852.2:p.Phe99Tyr
NM_001293197.2:c.80T>A (STUB1)	NP_001280126.1:p.Phe27Tyr