Canonical Allele Identifier: CA432356391

Gene: CAV3 SSUH2

Linked Data

• ClinVar Variation Id: 1099610
• ClinVar RCV Id: RCV001421935 ; RCV002384624
• dbSNP Id: rs2124977096
• MyVariant Identifiers: chr3:g.8775571A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8733885A>G , CM000665.2:g.8733885A>G	GRCh38
NC_000003.11:g.8775571A>G , CM000665.1:g.8775571A>G	GRCh37
NC_000003.10:g.8750571A>G	NCBI36
NG_008797.2:g.5076A>G , LRG_329:g.5076A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343849.3:c.9A>G (CAV3) MANE Select	ENSP00000341940.2:p.Ala3=
ENST00000343849.2:c.9A>G (CAV3)	ENSP00000341940.2:p.Ala3=
ENST00000397368.2:c.9A>G (CAV3)	ENSP00000380525.2:p.Ala3=
ENST00000435138.5:c.64+8574T>C (SSUH2)	ENSP00000412333.1:n.64+8574T>C
ENST00000472766.1:n.50A>G (CAV3)
ENST00000478513.1:n.335+8574T>C (SSUH2)
NM_001234.4:c.9A>G (CAV3)	NP_001225.1:p.Ala3=
NM_033337.2:c.9A>G , LRG_329t1:c.9A>G (CAV3)	NP_203123.1:p.Ala3=
XR_940435.1:n.330+8574T>C (SSUH2)
XM_017006530.1:c.-283+8574T>C (SSUH2)	XP_016862019.1:n.-283+8574T>C
NM_001234.5:c.9A>G (CAV3)	NP_001225.1:p.Ala3=
NM_033337.3:c.9A>G (CAV3) MANE Select	NP_203123.1:p.Ala3=