Canonical Allele Identifier: CA2755144095

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8734383dup , CM000665.2:g.8734383dup GRCh38
NC_000003.11:g.8776069dup , CM000665.1:g.8776069dup GRCh37
NC_000003.10:g.8751069dup NCBI36
NG_008797.2:g.5574dup , LRG_329:g.5574dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343849.3:c.114+393dup (CAV3) MANE Select ENSP00000341940.2:n.114+393dup
ENST00000343849.2:c.114+393dup (CAV3) ENSP00000341940.2:n.114+393dup
ENST00000397368.2:c.114+393dup (CAV3) ENSP00000380525.2:n.114+393dup
ENST00000435138.5:c.64+8077dup (SSUH2) ENSP00000412333.1:n.64+8077dup
ENST00000472766.1:n.155+393dup (CAV3)
ENST00000478513.1:n.335+8077dup (SSUH2)
NM_001234.4:c.114+393dup (CAV3) NP_001225.1:n.114+393dup
NM_033337.2:c.114+393dup , LRG_329t1:c.114+393dup (CAV3) NP_203123.1:n.114+393dup
XR_940435.1:n.330+8077dup (SSUH2)
XM_017006530.1:c.-283+8077dup (SSUH2) XP_016862019.1:n.-283+8077dup
NM_001234.5:c.114+393dup (CAV3) NP_001225.1:n.114+393dup
NM_033337.3:c.114+393dup (CAV3) MANE Select NP_203123.1:n.114+393dup