Canonical Allele Identifier: CA215212
Gene: CAV3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31742
ClinVar RCV Id: RCV000024428
dbSNP Id: rs199476338

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8745718_8745723del , CM000665.2:g.8745718_8745723del GRCh38
NC_000003.11:g.8787404_8787409del , CM000665.1:g.8787404_8787409del GRCh37
NC_000003.10:g.8762404_8762409del NCBI36
NG_008797.2:g.16909_16914del , LRG_329:g.16909_16914del

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.307_312del MANE Select ENSP00000341940.2:p.Val103_Val104del
ENST00000343849.2:c.307_312del ENSP00000341940.2:p.Val103_Val104del
ENST00000397368.2:c.307_312del ENSP00000380525.2:p.Val103_Val104del
ENST00000472766.1:n.155+11728_155+11733del
NM_001234.4:c.307_312del NP_001225.1:p.Val103_Val104del
NM_033337.2:c.307_312del , LRG_329t1:c.307_312del NP_203123.1:p.Val103_Val104del
NM_001234.5:c.307_312del NP_001225.1:p.Val103_Val104del
NM_033337.3:c.307_312del MANE Select NP_203123.1:p.Val103_Val104del