Canonical Allele Identifier: CA394112131

Gene: STUB1 MSLN

Linked Data

• dbSNP Id: rs780472903
• gnomAD v2: 16-731491-G-A
• gnomAD v4: 16-681491-G-A
• MyVariant Identifiers: chr16:g.731491G>A (hg19) ; chr16:g.681491G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681491G>A , CM000678.2:g.681491G>A	GRCh38
NC_000016.9:g.731491G>A , CM000678.1:g.731491G>A	GRCh37
NC_000016.8:g.671492G>A	NCBI36
NG_034141.1:g.6381G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.412G>A (STUB1) MANE Select	ENSP00000219548.4:p.Ala138Thr
ENST00000219548.8:c.412G>A (STUB1)	ENSP00000219548.4:p.Ala138Thr
ENST00000563505.5:n.508G>A (STUB1)
ENST00000564316.1:c.11G>A (STUB1)
ENST00000564370.5:c.196G>A (STUB1)	ENSP00000456875.1:p.Ala66Thr
ENST00000565677.5:c.196G>A (STUB1)	ENSP00000457228.1:p.Ala66Thr
ENST00000566181.2:n.181G>A (STUB1)
ENST00000566408.5:c.129G>A (STUB1)
ENST00000567173.5:c.355G>A (STUB1)	ENSP00000456591.1:p.Ala119Thr
ENST00000569248.5:n.986G>A (STUB1)
ENST00000620831.4:c.-50+38188G>A (MSLN)	ENSP00000482893.1:n.-50+38188G>A
NM_001293197.1:c.196G>A (STUB1)	NP_001280126.1:p.Ala66Thr
NM_005861.3:c.412G>A (STUB1)	NP_005852.2:p.Ala138Thr
NM_005861.4:c.412G>A (STUB1) MANE Select	NP_005852.2:p.Ala138Thr
NM_001293197.2:c.196G>A (STUB1)	NP_001280126.1:p.Ala66Thr