Canonical Allele Identifier: CA2630853803

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681291_681360del , CM000678.2:g.681291_681360del GRCh38
NC_000016.9:g.731291_731360del , CM000678.1:g.731291_731360del GRCh37
NC_000016.8:g.671292_671361del NCBI36
NG_034141.1:g.6181_6250del

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.299_358+10del (STUB1)
ENST00000219548.8:c.299_358+10del (STUB1)
ENST00000563505.5:n.395_454+10del (STUB1)
ENST00000564370.5:c.83_142+10del (STUB1)
ENST00000565677.5:c.83_142+10del (STUB1)
ENST00000566181.2:n.68_127+10del (STUB1)
ENST00000566408.5:c.16_75+10del (STUB1)
ENST00000567173.5:c.242_301+10del (STUB1)
ENST00000567790.1:n.329_398del (STUB1)
ENST00000569248.5:n.873_932+10del (STUB1)
ENST00000620831.4:c.-50+37988_-50+38057del (MSLN) ENSP00000482893.1:n.-50+37988_-50+38057del
NM_001293197.1:c.83_142+10del (STUB1)
NM_005861.3:c.299_358+10del (STUB1)
NM_005861.4:c.299_358+10del (STUB1)
NM_001293197.2:c.83_142+10del (STUB1)