Canonical Allele Identifier: CA911558542

Linked Data

dbSNP Id: rs1485718512

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8738771C>T , CM000665.2:g.8738771C>T GRCh38
NC_000003.11:g.8780457C>T , CM000665.1:g.8780457C>T GRCh37
NC_000003.10:g.8755457C>T NCBI36
NG_008797.2:g.9962C>T , LRG_329:g.9962C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.114+4781C>T (CAV3) MANE Select ENSP00000341940.2:n.114+4781C>T
ENST00000343849.2:c.114+4781C>T (CAV3) ENSP00000341940.2:n.114+4781C>T
ENST00000397368.2:c.114+4781C>T (CAV3) ENSP00000380525.2:n.114+4781C>T
ENST00000435138.5:c.64+3688G>A (SSUH2) ENSP00000412333.1:n.64+3688G>A
ENST00000472766.1:n.155+4781C>T (CAV3)
ENST00000478513.1:n.335+3688G>A (SSUH2)
NM_001234.4:c.114+4781C>T (CAV3) NP_001225.1:n.114+4781C>T
NM_033337.2:c.114+4781C>T , LRG_329t1:c.114+4781C>T (CAV3) NP_203123.1:n.114+4781C>T
XR_940435.1:n.330+3688G>A (SSUH2)
XM_017006530.1:c.-283+3688G>A (SSUH2) XP_016862019.1:n.-283+3688G>A
NM_001234.5:c.114+4781C>T (CAV3) NP_001225.1:n.114+4781C>T
NM_033337.3:c.114+4781C>T (CAV3) MANE Select NP_203123.1:n.114+4781C>T