Canonical Allele Identifier: CA1950112668
Gene: CAVIN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319444C= , CM000673.2:g.6319444C= GRCh38
NC_000011.9:g.6340674C= , CM000673.1:g.6340674C= GRCh37
NC_000011.8:g.6297250C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.505G= MANE Select ENSP00000307292.3:p.Glu169=
ENST00000303927.3:c.505G= ENSP00000307292.3:p.Glu169=
ENST00000524852.1:n.291G=
ENST00000530979.1:c.601G= ENSP00000432047.1:p.Glu201=
ENST00000532354.1:n.527G=
NM_145040.2:c.505G= NP_659477.2:p.Glu169=
XR_930997.1:n.720+1224C=
XR_001748106.1:n.55C=
XR_242848.4:n.304C=
NM_145040.3:c.505G= MANE Select NP_659477.2:p.Glu169=