Canonical Allele Identifier: CA472720318
Gene: CAVIN3 HGNC NCBI

Linked Data

gnomAD v4: 11-6319172-A-G
MyVariant Identifiers: chr11:g.6340402A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319172A>G , CM000673.2:g.6319172A>G GRCh38
NC_000011.9:g.6340402A>G , CM000673.1:g.6340402A>G GRCh37
NC_000011.8:g.6296978A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.777T>C MANE Select ENSP00000307292.3:p.Ser259=
ENST00000303927.3:c.777T>C ENSP00000307292.3:p.Ser259=
ENST00000524852.1:n.563T>C
ENST00000530979.1:c.873T>C ENSP00000432047.1:p.Ser291=
ENST00000532354.1:n.799T>C
NM_145040.2:c.777T>C NP_659477.2:p.Ser259=
XR_930997.1:n.720+952A>G
XR_242848.4:n.32A>G
NM_145040.3:c.777T>C MANE Select NP_659477.2:p.Ser259=