Canonical Allele Identifier: CA620307629

Gene: STUB1 MSLN

Linked Data

• dbSNP Id: rs1441769660
• gnomAD v2: 16-731406-C-CGG
• gnomAD v4: 16-681406-C-CGG
• MyVariant Identifiers: chr16:g.731406_731407insGG (hg19) ; chr16:g.681406_681407insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681406_681407insGG , CM000678.2:g.681406_681407insGG	GRCh38
NC_000016.9:g.731406_731407insGG , CM000678.1:g.731406_731407insGG	GRCh37
NC_000016.8:g.671407_671408insGG	NCBI36
NG_034141.1:g.6296_6297insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.359-32_359-31insGG (STUB1) MANE Select	ENSP00000219548.4:n.359-32_359-31insGG
ENST00000219548.8:c.359-32_359-31insGG (STUB1)	ENSP00000219548.4:n.359-32_359-31insGG
ENST00000563505.5:n.455-32_455-31insGG (STUB1)
ENST00000564370.5:c.143-32_143-31insGG (STUB1)	ENSP00000456875.1:n.143-32_143-31insGG
ENST00000565677.5:c.143-32_143-31insGG (STUB1)	ENSP00000457228.1:n.143-32_143-31insGG
ENST00000566181.2:n.128-32_128-31insGG (STUB1)
ENST00000566408.5:c.76-32_76-31insGG (STUB1)
ENST00000567173.5:c.302-32_302-31insGG (STUB1)	ENSP00000456591.1:n.302-32_302-31insGG
ENST00000569248.5:n.933-32_933-31insGG (STUB1)
ENST00000620831.4:c.-50+38103_-50+38104insGG (MSLN)	ENSP00000482893.1:n.-50+38103_-50+38104insGG
NM_001293197.1:c.143-32_143-31insGG (STUB1)	NP_001280126.1:n.143-32_143-31insGG
NM_005861.3:c.359-32_359-31insGG (STUB1)	NP_005852.2:n.359-32_359-31insGG
NM_005861.4:c.359-32_359-31insGG (STUB1) MANE Select	NP_005852.2:n.359-32_359-31insGG
NM_001293197.2:c.143-32_143-31insGG (STUB1)	NP_001280126.1:n.143-32_143-31insGG