Canonical Allele Identifier: CA2201204429

Gene: STUB1 MSLN

Linked Data

• dbSNP Id: rs2039650200
• gnomAD v4: 16-681399-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681399G>A , CM000678.2:g.681399G>A	GRCh38
NC_000016.9:g.731399G>A , CM000678.1:g.731399G>A	GRCh37
NC_000016.8:g.671400G>A	NCBI36
NG_034141.1:g.6289G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.359-39G>A (STUB1) MANE Select	ENSP00000219548.4:n.359-39G>A
ENST00000219548.8:c.359-39G>A (STUB1)	ENSP00000219548.4:n.359-39G>A
ENST00000563505.5:n.455-39G>A (STUB1)
ENST00000564370.5:c.143-39G>A (STUB1)	ENSP00000456875.1:n.143-39G>A
ENST00000565677.5:c.143-39G>A (STUB1)	ENSP00000457228.1:n.143-39G>A
ENST00000566181.2:n.128-39G>A (STUB1)
ENST00000566408.5:c.76-39G>A (STUB1)
ENST00000567173.5:c.302-39G>A (STUB1)	ENSP00000456591.1:n.302-39G>A
ENST00000569248.5:n.933-39G>A (STUB1)
ENST00000620831.4:c.-50+38096G>A (MSLN)	ENSP00000482893.1:n.-50+38096G>A
NM_001293197.1:c.143-39G>A (STUB1)	NP_001280126.1:n.143-39G>A
NM_005861.3:c.359-39G>A (STUB1)	NP_005852.2:n.359-39G>A
NM_005861.4:c.359-39G>A (STUB1) MANE Select	NP_005852.2:n.359-39G>A
NM_001293197.2:c.143-39G>A (STUB1)	NP_001280126.1:n.143-39G>A