Canonical Allele Identifier: CA1950112558
Gene: CAVIN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319250C= , CM000673.2:g.6319250C= GRCh38
NC_000011.9:g.6340480C= , CM000673.1:g.6340480C= GRCh37
NC_000011.8:g.6297056C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.699G= MANE Select ENSP00000307292.3:p.Glu233=
ENST00000303927.3:c.699G= ENSP00000307292.3:p.Glu233=
ENST00000524852.1:n.485G=
ENST00000530979.1:c.795G= ENSP00000432047.1:p.Glu265=
ENST00000532354.1:n.721G=
NM_145040.2:c.699G= NP_659477.2:p.Glu233=
XR_930997.1:n.720+1030C=
XR_242848.4:n.110C=
NM_145040.3:c.699G= MANE Select NP_659477.2:p.Glu233=