Canonical Allele Identifier: CA2695221283

Gene: STUB1 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681505_681520delinsT , CM000678.2:g.681505_681520delinsT	GRCh38
NC_000016.9:g.731505_731520delinsT , CM000678.1:g.731505_731520delinsT	GRCh37
NC_000016.8:g.671506_671521delinsT	NCBI36
NG_034141.1:g.6395_6410delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.426_441delinsT (STUB1) MANE Select	ENSP00000219548.4:p.Lys143_Trp147del
ENST00000219548.8:c.426_441delinsT (STUB1)	ENSP00000219548.4:p.Lys143_Trp147del
ENST00000563505.5:n.522_537delinsT (STUB1)
ENST00000564316.1:c.25_40delinsT (STUB1)
ENST00000564370.5:c.210_225delinsT (STUB1)	ENSP00000456875.1:p.Lys71_Trp75del
ENST00000565677.5:c.210_225delinsT (STUB1)	ENSP00000457228.1:p.Lys71_Trp75del
ENST00000566181.2:n.195_210delinsT (STUB1)
ENST00000566408.5:c.143_158delinsT (STUB1)
ENST00000567173.5:c.369_384delinsT (STUB1)	ENSP00000456591.1:p.Lys124_Trp128del
ENST00000569248.5:n.1000_1015delinsT (STUB1)
ENST00000620831.4:c.-50+38202_-50+38217delinsT (MSLN)	ENSP00000482893.1:n.-50+38202_-50+38217delinsT
NM_001293197.1:c.210_225delinsT (STUB1)	NP_001280126.1:p.Lys71_Trp75del
NM_005861.3:c.426_441delinsT (STUB1)	NP_005852.2:p.Lys143_Trp147del
NM_005861.4:c.426_441delinsT (STUB1) MANE Select	NP_005852.2:p.Lys143_Trp147del
NM_001293197.2:c.210_225delinsT (STUB1)	NP_001280126.1:p.Lys71_Trp75del