Canonical Allele Identifier: CA394112506

Gene: STUB1 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.731565C>A (hg19) ; chr16:g.681565C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681565C>A , CM000678.2:g.681565C>A	GRCh38
NC_000016.9:g.731565C>A , CM000678.1:g.731565C>A	GRCh37
NC_000016.8:g.671566C>A	NCBI36
NG_034141.1:g.6455C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.486C>A (STUB1) MANE Select	ENSP00000219548.4:p.His162Gln
ENST00000219548.8:c.486C>A (STUB1)	ENSP00000219548.4:p.His162Gln
ENST00000563505.5:n.582C>A (STUB1)
ENST00000564316.1:c.85C>A (STUB1)
ENST00000564370.5:c.270C>A (STUB1)	ENSP00000456875.1:p.His90Gln
ENST00000565677.5:c.270C>A (STUB1)	ENSP00000457228.1:p.His90Gln
ENST00000566181.2:n.255C>A (STUB1)
ENST00000566408.5:c.203C>A (STUB1)
ENST00000567173.5:c.429C>A (STUB1)	ENSP00000456591.1:p.His143Gln
ENST00000569248.5:n.1060C>A (STUB1)
ENST00000620831.4:c.-50+38262C>A (MSLN)	ENSP00000482893.1:n.-50+38262C>A
NM_001293197.1:c.270C>A (STUB1)	NP_001280126.1:p.His90Gln
NM_005861.3:c.486C>A (STUB1)	NP_005852.2:p.His162Gln
NM_005861.4:c.486C>A (STUB1) MANE Select	NP_005852.2:p.His162Gln
NM_001293197.2:c.270C>A (STUB1)	NP_001280126.1:p.His90Gln