Canonical Allele Identifier: CA916830612

Linked Data

dbSNP Id: rs1559645503

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8738419_8738420insTTGTGCCCT , CM000665.2:g.8738419_8738420insTTGTGCCCT GRCh38
NC_000003.11:g.8780105_8780106insTTGTGCCCT , CM000665.1:g.8780105_8780106insTTGTGCCCT GRCh37
NC_000003.10:g.8755105_8755106insTTGTGCCCT NCBI36
NG_008797.2:g.9610_9611insTTGTGCCCT , LRG_329:g.9610_9611insTTGTGCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000343849.3:c.114+4429_114+4430insTTGTGCCCT (CAV3) MANE Select ENSP00000341940.2:n.114+4429_114+4430insTTGTGCCCT
ENST00000343849.2:c.114+4429_114+4430insTTGTGCCCT (CAV3) ENSP00000341940.2:n.114+4429_114+4430insTTGTGCCCT
ENST00000397368.2:c.114+4429_114+4430insTTGTGCCCT (CAV3) ENSP00000380525.2:n.114+4429_114+4430insTTGTGCCCT
ENST00000435138.5:c.64+4043_64+4044insCACAAAGGG (SSUH2) ENSP00000412333.1:n.64+4043_64+4044insCACAAAGGG
ENST00000472766.1:n.155+4429_155+4430insTTGTGCCCT (CAV3)
ENST00000478513.1:n.335+4043_335+4044insCACAAAGGG (SSUH2)
NM_001234.4:c.114+4429_114+4430insTTGTGCCCT (CAV3) NP_001225.1:n.114+4429_114+4430insTTGTGCCCT
NM_033337.2:c.114+4429_114+4430insTTGTGCCCT , LRG_329t1:c.114+4429_114+4430insTTGTGCCCT (CAV3) NP_203123.1:n.114+4429_114+4430insTTGTGCCCT
XR_940435.1:n.330+4043_330+4044insCACAAAGGG (SSUH2)
XM_017006530.1:c.-283+4043_-283+4044insCACAAAGGG (SSUH2) XP_016862019.1:n.-283+4043_-283+4044insCACAAAGGG
NM_001234.5:c.114+4429_114+4430insTTGTGCCCT (CAV3) NP_001225.1:n.114+4429_114+4430insTTGTGCCCT
NM_033337.3:c.114+4429_114+4430insTTGTGCCCT (CAV3) MANE Select NP_203123.1:n.114+4429_114+4430insTTGTGCCCT