Canonical Allele Identifier: CA472908949
Gene: CAVIN3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.6340687C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319457C>T , CM000673.2:g.6319457C>T GRCh38
NC_000011.9:g.6340687C>T , CM000673.1:g.6340687C>T GRCh37
NC_000011.8:g.6297263C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.492G>A MANE Select ENSP00000307292.3:p.Glu164=
ENST00000303927.3:c.492G>A ENSP00000307292.3:p.Glu164=
ENST00000524852.1:n.278G>A
ENST00000530979.1:c.588G>A ENSP00000432047.1:p.Glu196=
ENST00000532354.1:n.514G>A
NM_145040.2:c.492G>A NP_659477.2:p.Glu164=
XR_930997.1:n.720+1237C>T
XR_001748106.1:n.68C>T
XR_242848.4:n.317C>T
NM_145040.3:c.492G>A MANE Select NP_659477.2:p.Glu164=