Canonical Allele Identifier: CA1950112700
Gene: CAVIN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319498A= , CM000673.2:g.6319498A= GRCh38
NC_000011.9:g.6340728A= , CM000673.1:g.6340728A= GRCh37
NC_000011.8:g.6297304A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.451T= MANE Select ENSP00000307292.3:p.Ser151=
ENST00000303927.3:c.451T= ENSP00000307292.3:p.Ser151=
ENST00000524852.1:n.237T=
ENST00000530979.1:c.547T= ENSP00000432047.1:p.Ser183=
ENST00000532354.1:n.473T=
NM_145040.2:c.451T= NP_659477.2:p.Ser151=
XR_930997.1:n.720+1278A=
XR_001748106.1:n.109A=
XR_242848.4:n.358A=
NM_145040.3:c.451T= MANE Select NP_659477.2:p.Ser151=