Canonical Allele Identifier: CA2201204410

Gene: STUB1 MSLN

Linked Data

• dbSNP Id: rs2039649729

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681384_681385del , CM000678.2:g.681384_681385del	GRCh38
NC_000016.9:g.731384_731385del , CM000678.1:g.731384_731385del	GRCh37
NC_000016.8:g.671385_671386del	NCBI36
NG_034141.1:g.6274_6275del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.358+34_358+35del (STUB1) MANE Select	ENSP00000219548.4:n.358+34_358+35del
ENST00000219548.8:c.358+34_358+35del (STUB1)	ENSP00000219548.4:n.358+34_358+35del
ENST00000563505.5:n.454+34_454+35del (STUB1)
ENST00000564370.5:c.142+34_142+35del (STUB1)	ENSP00000456875.1:n.142+34_142+35del
ENST00000565677.5:c.142+34_142+35del (STUB1)	ENSP00000457228.1:n.142+34_142+35del
ENST00000566181.2:n.127+34_127+35del (STUB1)
ENST00000566408.5:c.75+34_75+35del (STUB1)
ENST00000567173.5:c.301+34_301+35del (STUB1)	ENSP00000456591.1:n.301+34_301+35del
ENST00000567790.1:n.422_423del (STUB1)
ENST00000569248.5:n.932+34_932+35del (STUB1)
ENST00000620831.4:c.-50+38081_-50+38082del (MSLN)	ENSP00000482893.1:n.-50+38081_-50+38082del
NM_001293197.1:c.142+34_142+35del (STUB1)	NP_001280126.1:n.142+34_142+35del
NM_005861.3:c.358+34_358+35del (STUB1)	NP_005852.2:n.358+34_358+35del
NM_005861.4:c.358+34_358+35del (STUB1) MANE Select	NP_005852.2:n.358+34_358+35del
NM_001293197.2:c.142+34_142+35del (STUB1)	NP_001280126.1:n.142+34_142+35del