Canonical Allele Identifier: CA1344403908

Linked Data

dbSNP Id: rs1707965344

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8741715_8741724del , CM000665.2:g.8741715_8741724del GRCh38
NC_000003.11:g.8783401_8783410del , CM000665.1:g.8783401_8783410del GRCh37
NC_000003.10:g.8758401_8758410del NCBI36
NG_008797.2:g.12906_12915del , LRG_329:g.12906_12915del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343849.3:c.115-3811_115-3802del (CAV3) MANE Select ENSP00000341940.2:n.115-3811_115-3802del
ENST00000343849.2:c.115-3811_115-3802del (CAV3) ENSP00000341940.2:n.115-3811_115-3802del
ENST00000397368.2:c.115-3811_115-3802del (CAV3) ENSP00000380525.2:n.115-3811_115-3802del
ENST00000435138.5:c.64+738_64+747del (SSUH2) ENSP00000412333.1:n.64+738_64+747del
ENST00000472766.1:n.155+7725_155+7734del (CAV3)
ENST00000478513.1:n.335+738_335+747del (SSUH2)
NM_001234.4:c.115-3811_115-3802del (CAV3) NP_001225.1:n.115-3811_115-3802del
NM_033337.2:c.115-3811_115-3802del , LRG_329t1:c.115-3811_115-3802del (CAV3) NP_203123.1:n.115-3811_115-3802del
XR_940435.1:n.330+738_330+747del (SSUH2)
XM_017006530.1:c.-283+738_-283+747del (SSUH2) XP_016862019.1:n.-283+738_-283+747del
NM_001234.5:c.115-3811_115-3802del (CAV3) NP_001225.1:n.115-3811_115-3802del
NM_033337.3:c.115-3811_115-3802del (CAV3) MANE Select NP_203123.1:n.115-3811_115-3802del