Canonical Allele Identifier: CA2201204388

Gene: STUB1 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681364C= , CM000678.2:g.681364C=	GRCh38
NC_000016.9:g.731364C= , CM000678.1:g.731364C=	GRCh37
NC_000016.8:g.671365C=	NCBI36
NG_034141.1:g.6254C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.358+14C= (STUB1) MANE Select	ENSP00000219548.4:n.358+14C=
ENST00000219548.8:c.358+14C= (STUB1)	ENSP00000219548.4:n.358+14C=
ENST00000563505.5:n.454+14C= (STUB1)
ENST00000564370.5:c.142+14C= (STUB1)	ENSP00000456875.1:n.142+14C=
ENST00000565677.5:c.142+14C= (STUB1)	ENSP00000457228.1:n.142+14C=
ENST00000566181.2:n.127+14C= (STUB1)
ENST00000566408.5:c.75+14C= (STUB1)
ENST00000567173.5:c.301+14C= (STUB1)	ENSP00000456591.1:n.301+14C=
ENST00000567790.1:n.402C= (STUB1)
ENST00000569248.5:n.932+14C= (STUB1)
ENST00000620831.4:c.-50+38061C= (MSLN)	ENSP00000482893.1:n.-50+38061C=
NM_001293197.1:c.142+14C= (STUB1)	NP_001280126.1:n.142+14C=
NM_005861.3:c.358+14C= (STUB1)	NP_005852.2:n.358+14C=
NM_005861.4:c.358+14C= (STUB1) MANE Select	NP_005852.2:n.358+14C=
NM_001293197.2:c.142+14C= (STUB1)	NP_001280126.1:n.142+14C=