Canonical Allele Identifier: CA472720332
Gene: CAVIN3 HGNC NCBI

Linked Data

gnomAD v4: 11-6319199-G-T
MyVariant Identifiers: chr11:g.6340429G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319199G>T , CM000673.2:g.6319199G>T GRCh38
NC_000011.9:g.6340429G>T , CM000673.1:g.6340429G>T GRCh37
NC_000011.8:g.6297005G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000303927.4:c.750C>A MANE Select ENSP00000307292.3:p.Ala250=
ENST00000303927.3:c.750C>A ENSP00000307292.3:p.Ala250=
ENST00000524852.1:n.536C>A
ENST00000530979.1:c.846C>A ENSP00000432047.1:p.Ala282=
ENST00000532354.1:n.772C>A
NM_145040.2:c.750C>A NP_659477.2:p.Ala250=
XR_930997.1:n.720+979G>T
XR_242848.4:n.59G>T
NM_145040.3:c.750C>A MANE Select NP_659477.2:p.Ala250=