Canonical Allele Identifier: CA2577496477

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733883del , CM000665.2:g.8733883del GRCh38
NC_000003.11:g.8775569del , CM000665.1:g.8775569del GRCh37
NC_000003.10:g.8750569del NCBI36
NG_008797.2:g.5074del , LRG_329:g.5074del

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.7del (CAV3) MANE Select ENSP00000341940.2:p.Ala3GlnfsTer23
ENST00000343849.2:c.7del (CAV3) ENSP00000341940.2:p.Ala3GlnfsTer23
ENST00000397368.2:c.7del (CAV3) ENSP00000380525.2:p.Ala3GlnfsTer23
ENST00000435138.5:c.64+8577del (SSUH2) ENSP00000412333.1:n.64+8577del
ENST00000472766.1:n.48del (CAV3)
ENST00000478513.1:n.335+8577del (SSUH2)
NM_001234.4:c.7del (CAV3) NP_001225.1:p.Ala3GlnfsTer23
NM_033337.2:c.7del , LRG_329t1:c.7del (CAV3) NP_203123.1:p.Ala3GlnfsTer23
XR_940435.1:n.330+8577del (SSUH2)
XM_017006530.1:c.-283+8577del (SSUH2) XP_016862019.1:n.-283+8577del
NM_001234.5:c.7del (CAV3) NP_001225.1:p.Ala3GlnfsTer23
NM_033337.3:c.7del (CAV3) MANE Select NP_203123.1:p.Ala3GlnfsTer23