Canonical Allele Identifier: CA2630854527

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681533_681535del , CM000678.2:g.681533_681535del GRCh38
NC_000016.9:g.731533_731535del , CM000678.1:g.731533_731535del GRCh37
NC_000016.8:g.671534_671536del NCBI36
NG_034141.1:g.6423_6425del

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.454_456del (STUB1) MANE Select ENSP00000219548.4:p.Glu152del
ENST00000219548.8:c.454_456del (STUB1) ENSP00000219548.4:p.Glu152del
ENST00000563505.5:n.550_552del (STUB1)
ENST00000564316.1:c.53_55del (STUB1)
ENST00000564370.5:c.238_240del (STUB1) ENSP00000456875.1:p.Glu80del
ENST00000565677.5:c.238_240del (STUB1) ENSP00000457228.1:p.Glu80del
ENST00000566181.2:n.223_225del (STUB1)
ENST00000566408.5:c.171_173del (STUB1)
ENST00000567173.5:c.397_399del (STUB1) ENSP00000456591.1:p.Glu133del
ENST00000569248.5:n.1028_1030del (STUB1)
ENST00000620831.4:c.-50+38230_-50+38232del (MSLN) ENSP00000482893.1:n.-50+38230_-50+38232del
NM_001293197.1:c.238_240del (STUB1) NP_001280126.1:p.Glu80del
NM_005861.3:c.454_456del (STUB1) NP_005852.2:p.Glu152del
NM_005861.4:c.454_456del (STUB1) MANE Select NP_005852.2:p.Glu152del
NM_001293197.2:c.238_240del (STUB1) NP_001280126.1:p.Glu80del