Canonical Allele Identifier: CA891842703

Linked Data

ClinVar Variation Id: 577351
ClinVar RCV Id: RCV000700082
dbSNP Id: rs1559640153

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733975_8733978delinsT , CM000665.2:g.8733975_8733978delinsT GRCh38
NC_000003.11:g.8775661_8775664delinsT , CM000665.1:g.8775661_8775664delinsT GRCh37
NC_000003.10:g.8750661_8750664delinsT NCBI36
NG_008797.2:g.5166_5169delinsT , LRG_329:g.5166_5169delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.99_102delinsT (CAV3) MANE Select ENSP00000341940.2:p.Glu34del
ENST00000343849.2:c.99_102delinsT (CAV3) ENSP00000341940.2:p.Glu34del
ENST00000397368.2:c.99_102delinsT (CAV3) ENSP00000380525.2:p.Glu34del
ENST00000435138.5:c.64+8481_64+8484delinsA (SSUH2) ENSP00000412333.1:n.64+8481_64+8484delins...
ENST00000472766.1:n.140_143delinsT (CAV3)
ENST00000478513.1:n.335+8481_335+8484delinsA (SSUH2)
NM_001234.4:c.99_102delinsT (CAV3) NP_001225.1:p.Glu34del
NM_033337.2:c.99_102delinsT , LRG_329t1:c.99_102delinsT (CAV3) NP_203123.1:p.Glu34del
XR_940435.1:n.330+8481_330+8484delinsA (SSUH2)
XM_017006530.1:c.-283+8481_-283+8484delinsA (SSUH2) XP_016862019.1:n.-283+8481_-283+8484delin...
NM_001234.5:c.99_102delinsT (CAV3) NP_001225.1:p.Glu34del
NM_033337.3:c.99_102delinsT (CAV3) MANE Select NP_203123.1:p.Glu34del