Canonical Allele Identifier: CA2201204528

Gene: STUB1 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681504_681507delinsCGAA , CM000678.2:g.681504_681507delinsCGAA	GRCh38
NC_000016.9:g.731504_731507delinsCGAA , CM000678.1:g.731504_731507delinsCGAA	GRCh37
NC_000016.8:g.671505_671508delinsCGAA	NCBI36
NG_034141.1:g.6394_6397delinsCGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.425_428delinsCGAA (STUB1) MANE Select	ENSP00000219548.4:p.Ala142=
ENST00000219548.8:c.425_428delinsCGAA (STUB1)	ENSP00000219548.4:p.Ala142=
ENST00000563505.5:n.521_524delinsCGAA (STUB1)
ENST00000564316.1:c.24_27delinsCGAA (STUB1)
ENST00000564370.5:c.209_212delinsCGAA (STUB1)	ENSP00000456875.1:p.Ala70=
ENST00000565677.5:c.209_212delinsCGAA (STUB1)	ENSP00000457228.1:p.Ala70=
ENST00000566181.2:n.194_197delinsCGAA (STUB1)
ENST00000566408.5:c.142_145delinsCGAA (STUB1)
ENST00000567173.5:c.368_371delinsCGAA (STUB1)	ENSP00000456591.1:p.Ala123=
ENST00000569248.5:n.999_1002delinsCGAA (STUB1)
ENST00000620831.4:c.-50+38201_-50+38204delinsCGAA (MSLN)	ENSP00000482893.1:n.-50+38201_-50+38204delinsCGAA
NM_001293197.1:c.209_212delinsCGAA (STUB1)	NP_001280126.1:p.Ala70=
NM_005861.3:c.425_428delinsCGAA (STUB1)	NP_005852.2:p.Ala142=
NM_005861.4:c.425_428delinsCGAA (STUB1) MANE Select	NP_005852.2:p.Ala142=
NM_001293197.2:c.209_212delinsCGAA (STUB1)	NP_001280126.1:p.Ala70=