Canonical Allele Identifier: CA1950112431
Gene: CAVIN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319029T= , CM000673.2:g.6319029T= GRCh38
NC_000011.9:g.6340259T= , CM000673.1:g.6340259T= GRCh37
NC_000011.8:g.6296835T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.*134A= MANE Select ENSP00000307292.3:n.*134A=
ENST00000303927.3:c.*134A= ENSP00000307292.3:n.*134A=
ENST00000532354.1:n.942A=
NM_145040.2:c.*134A= NP_659477.2:n.*134A=
XR_930997.1:n.720+809T=
NM_145040.3:c.*134A= MANE Select NP_659477.2:n.*134A=