Canonical Allele Identifier: CA394112317

Gene: STUB1 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.731527A>G (hg19) ; chr16:g.681527A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681527A>G , CM000678.2:g.681527A>G	GRCh38
NC_000016.9:g.731527A>G , CM000678.1:g.731527A>G	GRCh37
NC_000016.8:g.671528A>G	NCBI36
NG_034141.1:g.6417A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.448A>G (STUB1) MANE Select	ENSP00000219548.4:p.Ile150Val
ENST00000219548.8:c.448A>G (STUB1)	ENSP00000219548.4:p.Ile150Val
ENST00000563505.5:n.544A>G (STUB1)
ENST00000564316.1:c.47A>G (STUB1)
ENST00000564370.5:c.232A>G (STUB1)	ENSP00000456875.1:p.Ile78Val
ENST00000565677.5:c.232A>G (STUB1)	ENSP00000457228.1:p.Ile78Val
ENST00000566181.2:n.217A>G (STUB1)
ENST00000566408.5:c.165A>G (STUB1)
ENST00000567173.5:c.391A>G (STUB1)	ENSP00000456591.1:p.Ile131Val
ENST00000569248.5:n.1022A>G (STUB1)
ENST00000620831.4:c.-50+38224A>G (MSLN)	ENSP00000482893.1:n.-50+38224A>G
NM_001293197.1:c.232A>G (STUB1)	NP_001280126.1:p.Ile78Val
NM_005861.3:c.448A>G (STUB1)	NP_005852.2:p.Ile150Val
NM_005861.4:c.448A>G (STUB1) MANE Select	NP_005852.2:p.Ile150Val
NM_001293197.2:c.232A>G (STUB1)	NP_001280126.1:p.Ile78Val