Canonical Allele Identifier: CA432525936

Gene: CAV3

Linked Data

• ClinVar Variation Id: 2165576
• ClinVar RCV Id: RCV003084440
• gnomAD v4: 3-8745637-T-C
• MyVariant Identifiers: chr3:g.8787323T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8745637T>C , CM000665.2:g.8745637T>C	GRCh38
NC_000003.11:g.8787323T>C , CM000665.1:g.8787323T>C	GRCh37
NC_000003.10:g.8762323T>C	NCBI36
NG_008797.2:g.16828T>C , LRG_329:g.16828T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343849.3:c.226T>C MANE Select	ENSP00000341940.2:p.Leu76=
ENST00000343849.2:c.226T>C	ENSP00000341940.2:p.Leu76=
ENST00000397368.2:c.226T>C	ENSP00000380525.2:p.Leu76=
ENST00000472766.1:n.155+11647T>C
NM_001234.4:c.226T>C	NP_001225.1:p.Leu76=
NM_033337.2:c.226T>C , LRG_329t1:c.226T>C	NP_203123.1:p.Leu76=
NM_001234.5:c.226T>C	NP_001225.1:p.Leu76=
NM_033337.3:c.226T>C MANE Select	NP_203123.1:p.Leu76=