Canonical Allele Identifier: CA351663384
Gene: CAV3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1377372
ClinVar RCV Id: RCV001889892
dbSNP Id: rs116840801
gnomAD v3: 3-8745668-T-A
gnomAD v4: 3-8745668-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8745668T>A , CM000665.2:g.8745668T>A GRCh38
NC_000003.11:g.8787354T>A , CM000665.1:g.8787354T>A GRCh37
NC_000003.10:g.8762354T>A NCBI36
NG_008797.2:g.16859T>A , LRG_329:g.16859T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343849.3:c.257T>A MANE Select ENSP00000341940.2:p.Leu86Gln
ENST00000343849.2:c.257T>A ENSP00000341940.2:p.Leu86Gln
ENST00000397368.2:c.257T>A ENSP00000380525.2:p.Leu86Gln
ENST00000472766.1:n.155+11678T>A
NM_001234.4:c.257T>A NP_001225.1:p.Leu86Gln
NM_033337.2:c.257T>A , LRG_329t1:c.257T>A NP_203123.1:p.Leu86Gln
NM_001234.5:c.257T>A NP_001225.1:p.Leu86Gln
NM_033337.3:c.257T>A MANE Select NP_203123.1:p.Leu86Gln