Canonical Allele Identifier: CA1950112485
Gene: CAVIN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319126A= , CM000673.2:g.6319126A= GRCh38
NC_000011.9:g.6340356A= , CM000673.1:g.6340356A= GRCh37
NC_000011.8:g.6296932A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.*37T= MANE Select ENSP00000307292.3:n.*37T=
ENST00000303927.3:c.*37T= ENSP00000307292.3:n.*37T=
ENST00000532354.1:n.845T=
NM_145040.2:c.*37T= NP_659477.2:n.*37T=
XR_930997.1:n.720+906A=
NM_145040.3:c.*37T= MANE Select NP_659477.2:n.*37T=