Canonical Allele Identifier: CA379352351
Gene: CAVIN3 HGNC NCBI

Linked Data

dbSNP Id: rs1846777368
gnomAD v4: 11-6319438-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6319438C>T , CM000673.2:g.6319438C>T GRCh38
NC_000011.9:g.6340668C>T , CM000673.1:g.6340668C>T GRCh37
NC_000011.8:g.6297244C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303927.4:c.511G>A MANE Select ENSP00000307292.3:p.Val171Met
ENST00000303927.3:c.511G>A ENSP00000307292.3:p.Val171Met
ENST00000524852.1:n.297G>A
ENST00000530979.1:c.607G>A ENSP00000432047.1:p.Val203Met
ENST00000532354.1:n.533G>A
NM_145040.2:c.511G>A NP_659477.2:p.Val171Met
XR_930997.1:n.720+1218C>T
XR_001748106.1:n.49C>T
XR_242848.4:n.298C>T
NM_145040.3:c.511G>A MANE Select NP_659477.2:p.Val171Met