Canonical Allele Identifier: CA2989033836

Gene: CAV3 SSUH2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8733986dup , CM000665.2:g.8733986dup	GRCh38
NC_000003.11:g.8775672dup , CM000665.1:g.8775672dup	GRCh37
NC_000003.10:g.8750672dup	NCBI36
NG_008797.2:g.5177dup , LRG_329:g.5177dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343849.3:c.110dup (CAV3) MANE Select	ENSP00000341940.2:p.Lys38GlnfsTer5
ENST00000343849.2:c.110dup (CAV3)	ENSP00000341940.2:p.Lys38GlnfsTer5
ENST00000397368.2:c.110dup (CAV3)	ENSP00000380525.2:p.Lys38GlnfsTer5
ENST00000435138.5:c.64+8473dup (SSUH2)	ENSP00000412333.1:n.64+8473dup
ENST00000472766.1:n.151dup (CAV3)
ENST00000478513.1:n.335+8473dup (SSUH2)
NM_001234.4:c.110dup (CAV3)	NP_001225.1:p.Lys38GlnfsTer5
NM_033337.2:c.110dup , LRG_329t1:c.110dup (CAV3)	NP_203123.1:p.Lys38GlnfsTer5
XR_940435.1:n.330+8473dup (SSUH2)
XM_017006530.1:c.-283+8473dup (SSUH2)	XP_016862019.1:n.-283+8473dup
NM_001234.5:c.110dup (CAV3)	NP_001225.1:p.Lys38GlnfsTer5
NM_033337.3:c.110dup (CAV3) MANE Select	NP_203123.1:p.Lys38GlnfsTer5