Canonical Allele Identifier: CA394112069

Gene: STUB1 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.731476G>T (hg19) ; chr16:g.681476G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681476G>T , CM000678.2:g.681476G>T	GRCh38
NC_000016.9:g.731476G>T , CM000678.1:g.731476G>T	GRCh37
NC_000016.8:g.671477G>T	NCBI36
NG_034141.1:g.6366G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.397G>T (STUB1) MANE Select	ENSP00000219548.4:p.Asp133Tyr
ENST00000219548.8:c.397G>T (STUB1)	ENSP00000219548.4:p.Asp133Tyr
ENST00000563505.5:n.493G>T (STUB1)
ENST00000564370.5:c.181G>T (STUB1)	ENSP00000456875.1:p.Asp61Tyr
ENST00000565677.5:c.181G>T (STUB1)	ENSP00000457228.1:p.Asp61Tyr
ENST00000566181.2:n.166G>T (STUB1)
ENST00000566408.5:c.114G>T (STUB1)
ENST00000567173.5:c.340G>T (STUB1)	ENSP00000456591.1:p.Asp114Tyr
ENST00000569248.5:n.971G>T (STUB1)
ENST00000620831.4:c.-50+38173G>T (MSLN)	ENSP00000482893.1:n.-50+38173G>T
NM_001293197.1:c.181G>T (STUB1)	NP_001280126.1:p.Asp61Tyr
NM_005861.3:c.397G>T (STUB1)	NP_005852.2:p.Asp133Tyr
NM_005861.4:c.397G>T (STUB1) MANE Select	NP_005852.2:p.Asp133Tyr
NM_001293197.2:c.181G>T (STUB1)	NP_001280126.1:p.Asp61Tyr