Canonical Allele Identifier: CA2840748432

Gene: STUB1 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681619dup , CM000678.2:g.681619dup	GRCh38
NC_000016.9:g.731619dup , CM000678.1:g.731619dup	GRCh37
NC_000016.8:g.671620dup	NCBI36
NG_034141.1:g.6509dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.524+16dup (STUB1) MANE Select	ENSP00000219548.4:n.524+16dup
ENST00000219548.8:c.524+16dup (STUB1)	ENSP00000219548.4:n.524+16dup
ENST00000563505.5:n.620+16dup (STUB1)
ENST00000564316.1:c.123+16dup (STUB1)
ENST00000564370.5:c.308+16dup (STUB1)	ENSP00000456875.1:n.308+16dup
ENST00000565677.5:c.308+16dup (STUB1)	ENSP00000457228.1:n.308+16dup
ENST00000566181.2:n.293+16dup (STUB1)
ENST00000566408.5:c.241+16dup (STUB1)
ENST00000567173.5:c.467+16dup (STUB1)	ENSP00000456591.1:n.467+16dup
ENST00000569248.5:n.1098+16dup (STUB1)
ENST00000620831.4:c.-50+38316dup (MSLN)	ENSP00000482893.1:n.-50+38316dup
NM_001293197.1:c.308+16dup (STUB1)	NP_001280126.1:n.308+16dup
NM_005861.3:c.524+16dup (STUB1)	NP_005852.2:n.524+16dup
NM_005861.4:c.524+16dup (STUB1) MANE Select	NP_005852.2:n.524+16dup
NM_001293197.2:c.308+16dup (STUB1)	NP_001280126.1:n.308+16dup