Canonical Allele Identifier: CA394112114

Gene: STUB1 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.731486C>A (hg19) ; chr16:g.681486C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681486C>A , CM000678.2:g.681486C>A	GRCh38
NC_000016.9:g.731486C>A , CM000678.1:g.731486C>A	GRCh37
NC_000016.8:g.671487C>A	NCBI36
NG_034141.1:g.6376C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.407C>A (STUB1) MANE Select	ENSP00000219548.4:p.Pro136His
ENST00000219548.8:c.407C>A (STUB1)	ENSP00000219548.4:p.Pro136His
ENST00000563505.5:n.503C>A (STUB1)
ENST00000564316.1:c.6C>A (STUB1)
ENST00000564370.5:c.191C>A (STUB1)	ENSP00000456875.1:p.Pro64His
ENST00000565677.5:c.191C>A (STUB1)	ENSP00000457228.1:p.Pro64His
ENST00000566181.2:n.176C>A (STUB1)
ENST00000566408.5:c.124C>A (STUB1)
ENST00000567173.5:c.350C>A (STUB1)	ENSP00000456591.1:p.Pro117His
ENST00000569248.5:n.981C>A (STUB1)
ENST00000620831.4:c.-50+38183C>A (MSLN)	ENSP00000482893.1:n.-50+38183C>A
NM_001293197.1:c.191C>A (STUB1)	NP_001280126.1:p.Pro64His
NM_005861.3:c.407C>A (STUB1)	NP_005852.2:p.Pro136His
NM_005861.4:c.407C>A (STUB1) MANE Select	NP_005852.2:p.Pro136His
NM_001293197.2:c.191C>A (STUB1)	NP_001280126.1:p.Pro64His