Canonical Allele Identifier: CA1344404061

Linked Data

dbSNP Id: rs1707977332

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8741996_8741998dup , CM000665.2:g.8741996_8741998dup GRCh38
NC_000003.11:g.8783682_8783684dup , CM000665.1:g.8783682_8783684dup GRCh37
NC_000003.10:g.8758682_8758684dup NCBI36
NG_008797.2:g.13187_13189dup , LRG_329:g.13187_13189dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343849.3:c.115-3530_115-3528dup (CAV3) MANE Select ENSP00000341940.2:n.115-3530_115-3528dup
ENST00000343849.2:c.115-3530_115-3528dup (CAV3) ENSP00000341940.2:n.115-3530_115-3528dup
ENST00000397368.2:c.115-3530_115-3528dup (CAV3) ENSP00000380525.2:n.115-3530_115-3528dup
ENST00000435138.5:c.64+461_64+463dup (SSUH2) ENSP00000412333.1:n.64+461_64+463dup
ENST00000472766.1:n.155+8006_155+8008dup (CAV3)
ENST00000478513.1:n.335+461_335+463dup (SSUH2)
NM_001234.4:c.115-3530_115-3528dup (CAV3) NP_001225.1:n.115-3530_115-3528dup
NM_033337.2:c.115-3530_115-3528dup , LRG_329t1:c.115-3530_115-3528dup (CAV3) NP_203123.1:n.115-3530_115-3528dup
XR_940435.1:n.330+461_330+463dup (SSUH2)
XM_017006530.1:c.-283+461_-283+463dup (SSUH2) XP_016862019.1:n.-283+461_-283+463dup
NM_001234.5:c.115-3530_115-3528dup (CAV3) NP_001225.1:n.115-3530_115-3528dup
NM_033337.3:c.115-3530_115-3528dup (CAV3) MANE Select NP_203123.1:n.115-3530_115-3528dup