Canonical Allele Identifier: CA69865028

Gene: CAV3 SSUH2

Linked Data

• dbSNP Id: rs35995175
• MyVariant Identifiers: chr3:g.8780443_8780444insA (hg19) ; chr3:g.8738757_8738758insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8738758dup , CM000665.2:g.8738758dup	GRCh38
NC_000003.11:g.8780444dup , CM000665.1:g.8780444dup	GRCh37
NC_000003.10:g.8755444dup	NCBI36
NG_008797.2:g.9949dup , LRG_329:g.9949dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000343849.3:c.114+4768dup (CAV3) MANE Select	ENSP00000341940.2:n.114+4768dup
ENST00000343849.2:c.114+4768dup (CAV3)	ENSP00000341940.2:n.114+4768dup
ENST00000397368.2:c.114+4768dup (CAV3)	ENSP00000380525.2:n.114+4768dup
ENST00000435138.5:c.64+3701dup (SSUH2)	ENSP00000412333.1:n.64+3701dup
ENST00000472766.1:n.155+4768dup (CAV3)
ENST00000478513.1:n.335+3701dup (SSUH2)
NM_001234.4:c.114+4768dup (CAV3)	NP_001225.1:n.114+4768dup
NM_033337.2:c.114+4768dup , LRG_329t1:c.114+4768dup (CAV3)	NP_203123.1:n.114+4768dup
XR_940435.1:n.330+3701dup (SSUH2)
XM_017006530.1:c.-283+3701dup (SSUH2)	XP_016862019.1:n.-283+3701dup
NM_001234.5:c.114+4768dup (CAV3)	NP_001225.1:n.114+4768dup
NM_033337.3:c.114+4768dup (CAV3) MANE Select	NP_203123.1:n.114+4768dup