Canonical Allele Identifier: CA379352002
Gene: CAVIN3 HGNC NCBI

Linked Data

gnomAD v4: 11-6319261-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319261G>A , CM000673.2:g.6319261G>A GRCh38
NC_000011.9:g.6340491G>A , CM000673.1:g.6340491G>A GRCh37
NC_000011.8:g.6297067G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.688C>T MANE Select ENSP00000307292.3:p.Pro230Ser
ENST00000303927.3:c.688C>T ENSP00000307292.3:p.Pro230Ser
ENST00000524852.1:n.474C>T
ENST00000530979.1:c.784C>T ENSP00000432047.1:p.Pro262Ser
ENST00000532354.1:n.710C>T
NM_145040.2:c.688C>T NP_659477.2:p.Pro230Ser
XR_930997.1:n.720+1041G>A
XR_242848.4:n.121G>A
NM_145040.3:c.688C>T MANE Select NP_659477.2:p.Pro230Ser