Canonical Allele Identifier: CA1344402326

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8738757G= , CM000665.2:g.8738757G= GRCh38
NC_000003.11:g.8780443G= , CM000665.1:g.8780443G= GRCh37
NC_000003.10:g.8755443G= NCBI36
NG_008797.2:g.9948G= , LRG_329:g.9948G=

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.114+4767G= (CAV3) MANE Select ENSP00000341940.2:n.114+4767G=
ENST00000343849.2:c.114+4767G= (CAV3) ENSP00000341940.2:n.114+4767G=
ENST00000397368.2:c.114+4767G= (CAV3) ENSP00000380525.2:n.114+4767G=
ENST00000435138.5:c.64+3702C= (SSUH2) ENSP00000412333.1:n.64+3702C=
ENST00000472766.1:n.155+4767G= (CAV3)
ENST00000478513.1:n.335+3702C= (SSUH2)
NM_001234.4:c.114+4767G= (CAV3) NP_001225.1:n.114+4767G=
NM_033337.2:c.114+4767G= , LRG_329t1:c.114+4767G= (CAV3) NP_203123.1:n.114+4767G=
XR_940435.1:n.330+3702C= (SSUH2)
XM_017006530.1:c.-283+3702C= (SSUH2) XP_016862019.1:n.-283+3702C=
NM_001234.5:c.114+4767G= (CAV3) NP_001225.1:n.114+4767G=
NM_033337.3:c.114+4767G= (CAV3) MANE Select NP_203123.1:n.114+4767G=