Canonical Allele Identifier: CA2201204576

Gene: STUB1 MSLN

Linked Data

• dbSNP Id: rs2039654013

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681549_681572del , CM000678.2:g.681549_681572del	GRCh38
NC_000016.9:g.731549_731572del , CM000678.1:g.731549_731572del	GRCh37
NC_000016.8:g.671550_671573del	NCBI36
NG_034141.1:g.6439_6462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.470_493del (STUB1) MANE Select	ENSP00000219548.4:p.Gln157_Tyr164del
ENST00000219548.8:c.470_493del (STUB1)	ENSP00000219548.4:p.Gln157_Tyr164del
ENST00000563505.5:n.566_589del (STUB1)
ENST00000564316.1:c.69_92del (STUB1)
ENST00000564370.5:c.254_277del (STUB1)	ENSP00000456875.1:p.Gln85_Tyr92del
ENST00000565677.5:c.254_277del (STUB1)	ENSP00000457228.1:p.Gln85_Tyr92del
ENST00000566181.2:n.239_262del (STUB1)
ENST00000566408.5:c.187_210del (STUB1)
ENST00000567173.5:c.413_436del (STUB1)	ENSP00000456591.1:p.Gln138_Tyr145del
ENST00000569248.5:n.1044_1067del (STUB1)
ENST00000620831.4:c.-50+38246_-50+38269del (MSLN)	ENSP00000482893.1:n.-50+38246_-50+38269del
NM_001293197.1:c.254_277del (STUB1)	NP_001280126.1:p.Gln85_Tyr92del
NM_005861.3:c.470_493del (STUB1)	NP_005852.2:p.Gln157_Tyr164del
NM_005861.4:c.470_493del (STUB1) MANE Select	NP_005852.2:p.Gln157_Tyr164del
NM_001293197.2:c.254_277del (STUB1)	NP_001280126.1:p.Gln85_Tyr92del