Canonical Allele Identifier: CA2514351789

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8734405del , CM000665.2:g.8734405del GRCh38
NC_000003.11:g.8776091del , CM000665.1:g.8776091del GRCh37
NC_000003.10:g.8751091del NCBI36
NG_008797.2:g.5596del , LRG_329:g.5596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343849.3:c.114+415del (CAV3) MANE Select ENSP00000341940.2:n.114+415del
ENST00000343849.2:c.114+415del (CAV3) ENSP00000341940.2:n.114+415del
ENST00000397368.2:c.114+415del (CAV3) ENSP00000380525.2:n.114+415del
ENST00000435138.5:c.64+8057del (SSUH2) ENSP00000412333.1:n.64+8057del
ENST00000472766.1:n.155+415del (CAV3)
ENST00000478513.1:n.335+8057del (SSUH2)
NM_001234.4:c.114+415del (CAV3) NP_001225.1:n.114+415del
NM_033337.2:c.114+415del , LRG_329t1:c.114+415del (CAV3) NP_203123.1:n.114+415del
XR_940435.1:n.330+8057del (SSUH2)
XM_017006530.1:c.-283+8057del (SSUH2) XP_016862019.1:n.-283+8057del
NM_001234.5:c.114+415del (CAV3) NP_001225.1:n.114+415del
NM_033337.3:c.114+415del (CAV3) MANE Select NP_203123.1:n.114+415del