Canonical Allele Identifier: CA215184
Gene: CAV3 HGNC NCBI
SSUH2 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.8733976G>A
GRCh37 chr3:g.8775662G>A
Revel Score:
ENST00000343849 (MANE Select) 0.672
ENST00000397368 0.672
gnomAD v2:
3:8775662 G / A
gnomAD v3:
3:8733976 G / A
gnomAD v4:
chr3-8733976-G-A
Joint Max Group AF 0.00002497 (NFE)
Genomes Max Group AF 0.00000488 (NFE)
Exomes Max Group AF 0.00002479 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733976G>A , CM000665.2:g.8733976G>A GRCh38
NC_000003.11:g.8775662G>A , CM000665.1:g.8775662G>A GRCh37
NC_000003.10:g.8750662G>A NCBI36
NG_008797.2:g.5167G>A , LRG_329:g.5167G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343849.3:c.100G>A (CAV3) MANE Select ENSP00000341940.2:p.Glu34Lys
ENST00000343849.2:c.100G>A (CAV3) ENSP00000341940.2:p.Glu34Lys
ENST00000397368.2:c.100G>A (CAV3) ENSP00000380525.2:p.Glu34Lys
ENST00000435138.5:c.64+8483C>T (SSUH2) ENSP00000412333.1:n.64+8483C>T
ENST00000472766.1:n.141G>A (CAV3)
ENST00000478513.1:n.335+8483C>T (SSUH2)
NM_001234.4:c.100G>A (CAV3) NP_001225.1:p.Glu34Lys
NM_033337.2:c.100G>A , LRG_329t1:c.100G>A (CAV3) NP_203123.1:p.Glu34Lys
XR_940435.1:n.330+8483C>T (SSUH2)
XM_017006530.1:c.-283+8483C>T (SSUH2) XP_016862019.1:n.-283+8483C>T
NM_001234.5:c.100G>A (CAV3) NP_001225.1:p.Glu34Lys
NM_033337.3:c.100G>A (CAV3) MANE Select NP_203123.1:p.Glu34Lys
Search 100 bp 5'
Search 100 bp 3'