Canonical Allele Identifier: CA1950112674
Gene: CAVIN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319452G= , CM000673.2:g.6319452G= GRCh38
NC_000011.9:g.6340682G= , CM000673.1:g.6340682G= GRCh37
NC_000011.8:g.6297258G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.497C= MANE Select ENSP00000307292.3:p.Ser166=
ENST00000303927.3:c.497C= ENSP00000307292.3:p.Ser166=
ENST00000524852.1:n.283C=
ENST00000530979.1:c.593C= ENSP00000432047.1:p.Ser198=
ENST00000532354.1:n.519C=
NM_145040.2:c.497C= NP_659477.2:p.Ser166=
XR_930997.1:n.720+1232G=
XR_001748106.1:n.63G=
XR_242848.4:n.312G=
NM_145040.3:c.497C= MANE Select NP_659477.2:p.Ser166=