Canonical Allele Identifier: CA295931

Gene: CAV3

Linked Data

• ClinVar Variation Id: 180794
• ClinVar RCV Id: RCV000157832 ; RCV000769180 ; RCV001037438 ; RCV003965173 ; RCV003162658
• dbSNP Id: rs559206877
• ExAC: 3:8787499 G / A
• gnomAD v2: 3-8787499-G-A
• gnomAD v4: 3-8745813-G-A
• MyVariant Identifiers: chr3:g.8787499G>A (hg19) ; chr3:g.8745813G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8745813G>A , CM000665.2:g.8745813G>A	GRCh38
NC_000003.11:g.8787499G>A , CM000665.1:g.8787499G>A	GRCh37
NC_000003.10:g.8762499G>A	NCBI36
NG_008797.2:g.17004G>A , LRG_329:g.17004G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343849.3:c.402G>A MANE Select	ENSP00000341940.2:p.Ala134=
ENST00000343849.2:c.402G>A	ENSP00000341940.2:p.Ala134=
ENST00000397368.2:c.402G>A	ENSP00000380525.2:p.Ala134=
ENST00000472766.1:n.155+11823G>A
NM_001234.4:c.402G>A	NP_001225.1:p.Ala134=
NM_033337.2:c.402G>A , LRG_329t1:c.402G>A	NP_203123.1:p.Ala134=
NM_001234.5:c.402G>A	NP_001225.1:p.Ala134=
NM_033337.3:c.402G>A MANE Select	NP_203123.1:p.Ala134=