Canonical Allele Identifier: CA2577496478

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733885del , CM000665.2:g.8733885del GRCh38
NC_000003.11:g.8775571del , CM000665.1:g.8775571del GRCh37
NC_000003.10:g.8750571del NCBI36
NG_008797.2:g.5076del , LRG_329:g.5076del

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.9del (CAV3) MANE Select ENSP00000341940.2:p.Glu4LysfsTer22
ENST00000343849.2:c.9del (CAV3) ENSP00000341940.2:p.Glu4LysfsTer22
ENST00000397368.2:c.9del (CAV3) ENSP00000380525.2:p.Glu4LysfsTer22
ENST00000435138.5:c.64+8574del (SSUH2) ENSP00000412333.1:n.64+8574del
ENST00000472766.1:n.50del (CAV3)
ENST00000478513.1:n.335+8574del (SSUH2)
NM_001234.4:c.9del (CAV3) NP_001225.1:p.Glu4LysfsTer22
NM_033337.2:c.9del , LRG_329t1:c.9del (CAV3) NP_203123.1:p.Glu4LysfsTer22
XR_940435.1:n.330+8574del (SSUH2)
XM_017006530.1:c.-283+8574del (SSUH2) XP_016862019.1:n.-283+8574del
NM_001234.5:c.9del (CAV3) NP_001225.1:p.Glu4LysfsTer22
NM_033337.3:c.9del (CAV3) MANE Select NP_203123.1:p.Glu4LysfsTer22