Canonical Allele Identifier: CA1950112477
Gene: CAVIN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319112A= , CM000673.2:g.6319112A= GRCh38
NC_000011.9:g.6340342A= , CM000673.1:g.6340342A= GRCh37
NC_000011.8:g.6296918A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000303927.4:c.*51T= MANE Select ENSP00000307292.3:n.*51T=
ENST00000303927.3:c.*51T= ENSP00000307292.3:n.*51T=
ENST00000532354.1:n.859T=
NM_145040.2:c.*51T= NP_659477.2:n.*51T=
XR_930997.1:n.720+892A=
NM_145040.3:c.*51T= MANE Select NP_659477.2:n.*51T=