Canonical Allele Identifier: CA394112408

Gene: STUB1 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.731545C>T (hg19) ; chr16:g.681545C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681545C>T , CM000678.2:g.681545C>T	GRCh38
NC_000016.9:g.731545C>T , CM000678.1:g.731545C>T	GRCh37
NC_000016.8:g.671546C>T	NCBI36
NG_034141.1:g.6435C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.466C>T (STUB1) MANE Select	ENSP00000219548.4:p.His156Tyr
ENST00000219548.8:c.466C>T (STUB1)	ENSP00000219548.4:p.His156Tyr
ENST00000563505.5:n.562C>T (STUB1)
ENST00000564316.1:c.65C>T (STUB1)
ENST00000564370.5:c.250C>T (STUB1)	ENSP00000456875.1:p.His84Tyr
ENST00000565677.5:c.250C>T (STUB1)	ENSP00000457228.1:p.His84Tyr
ENST00000566181.2:n.235C>T (STUB1)
ENST00000566408.5:c.183C>T (STUB1)
ENST00000567173.5:c.409C>T (STUB1)	ENSP00000456591.1:p.His137Tyr
ENST00000569248.5:n.1040C>T (STUB1)
ENST00000620831.4:c.-50+38242C>T (MSLN)	ENSP00000482893.1:n.-50+38242C>T
NM_001293197.1:c.250C>T (STUB1)	NP_001280126.1:p.His84Tyr
NM_005861.3:c.466C>T (STUB1)	NP_005852.2:p.His156Tyr
NM_005861.4:c.466C>T (STUB1) MANE Select	NP_005852.2:p.His156Tyr
NM_001293197.2:c.250C>T (STUB1)	NP_001280126.1:p.His84Tyr