Canonical Allele Identifier: CA351661300

Gene: CAV3 SSUH2

Linked Data

• ClinVar Variation Id: 2452813
• ClinVar RCV Id: RCV003177587 ; RCV003906666
• gnomAD v4: 3-8733913-A-G
• MyVariant Identifiers: chr3:g.8775599A>G (hg19) ; chr3:g.8733913A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8733913A>G , CM000665.2:g.8733913A>G	GRCh38
NC_000003.11:g.8775599A>G , CM000665.1:g.8775599A>G	GRCh37
NC_000003.10:g.8750599A>G	NCBI36
NG_008797.2:g.5104A>G , LRG_329:g.5104A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000343849.3:c.37A>G (CAV3) MANE Select	ENSP00000341940.2:p.Ile13Val
ENST00000343849.2:c.37A>G (CAV3)	ENSP00000341940.2:p.Ile13Val
ENST00000397368.2:c.37A>G (CAV3)	ENSP00000380525.2:p.Ile13Val
ENST00000435138.5:c.64+8546T>C (SSUH2)	ENSP00000412333.1:n.64+8546T>C
ENST00000472766.1:n.78A>G (CAV3)
ENST00000478513.1:n.335+8546T>C (SSUH2)
NM_001234.4:c.37A>G (CAV3)	NP_001225.1:p.Ile13Val
NM_033337.2:c.37A>G , LRG_329t1:c.37A>G (CAV3)	NP_203123.1:p.Ile13Val
XR_940435.1:n.330+8546T>C (SSUH2)
XM_017006530.1:c.-283+8546T>C (SSUH2)	XP_016862019.1:n.-283+8546T>C
NM_001234.5:c.37A>G (CAV3)	NP_001225.1:p.Ile13Val
NM_033337.3:c.37A>G (CAV3) MANE Select	NP_203123.1:p.Ile13Val