Canonical Allele Identifier: CA69867118

Linked Data

dbSNP Id: rs939398306

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8741928_8741934dup , CM000665.2:g.8741928_8741934dup GRCh38
NC_000003.11:g.8783614_8783620dup , CM000665.1:g.8783614_8783620dup GRCh37
NC_000003.10:g.8758614_8758620dup NCBI36
NG_008797.2:g.13119_13125dup , LRG_329:g.13119_13125dup

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.115-3598_115-3592dup (CAV3) MANE Select ENSP00000341940.2:n.115-3598_115-3592dup
ENST00000343849.2:c.115-3598_115-3592dup (CAV3) ENSP00000341940.2:n.115-3598_115-3592dup
ENST00000397368.2:c.115-3598_115-3592dup (CAV3) ENSP00000380525.2:n.115-3598_115-3592dup
ENST00000435138.5:c.64+525_64+531dup (SSUH2) ENSP00000412333.1:n.64+525_64+531dup
ENST00000472766.1:n.155+7938_155+7944dup (CAV3)
ENST00000478513.1:n.335+525_335+531dup (SSUH2)
NM_001234.4:c.115-3598_115-3592dup (CAV3) NP_001225.1:n.115-3598_115-3592dup
NM_033337.2:c.115-3598_115-3592dup , LRG_329t1:c.115-3598_115-3592dup (CAV3) NP_203123.1:n.115-3598_115-3592dup
XR_940435.1:n.330+525_330+531dup (SSUH2)
XM_017006530.1:c.-283+525_-283+531dup (SSUH2) XP_016862019.1:n.-283+525_-283+531dup
NM_001234.5:c.115-3598_115-3592dup (CAV3) NP_001225.1:n.115-3598_115-3592dup
NM_033337.3:c.115-3598_115-3592dup (CAV3) MANE Select NP_203123.1:n.115-3598_115-3592dup