Canonical Allele Identifier: CA1950112489
Gene: CAVIN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319132C= , CM000673.2:g.6319132C= GRCh38
NC_000011.9:g.6340362C= , CM000673.1:g.6340362C= GRCh37
NC_000011.8:g.6296938C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.*31G= MANE Select ENSP00000307292.3:n.*31G=
ENST00000303927.3:c.*31G= ENSP00000307292.3:n.*31G=
ENST00000524852.1:n.603G=
ENST00000532354.1:n.839G=
NM_145040.2:c.*31G= NP_659477.2:n.*31G=
XR_930997.1:n.720+912C=
NM_145040.3:c.*31G= MANE Select NP_659477.2:n.*31G=