Canonical Allele Identifier: CA540846321

Linked Data

dbSNP Id: rs1286931057
gnomAD v2: 3-8780324-A-G
gnomAD v3: 3-8738638-A-G
gnomAD v4: 3-8738638-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8738638A>G , CM000665.2:g.8738638A>G GRCh38
NC_000003.11:g.8780324A>G , CM000665.1:g.8780324A>G GRCh37
NC_000003.10:g.8755324A>G NCBI36
NG_008797.2:g.9829A>G , LRG_329:g.9829A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.114+4648A>G (CAV3) MANE Select ENSP00000341940.2:n.114+4648A>G
ENST00000343849.2:c.114+4648A>G (CAV3) ENSP00000341940.2:n.114+4648A>G
ENST00000397368.2:c.114+4648A>G (CAV3) ENSP00000380525.2:n.114+4648A>G
ENST00000435138.5:c.64+3821T>C (SSUH2) ENSP00000412333.1:n.64+3821T>C
ENST00000472766.1:n.155+4648A>G (CAV3)
ENST00000478513.1:n.335+3821T>C (SSUH2)
NM_001234.4:c.114+4648A>G (CAV3) NP_001225.1:n.114+4648A>G
NM_033337.2:c.114+4648A>G , LRG_329t1:c.114+4648A>G (CAV3) NP_203123.1:n.114+4648A>G
XR_940435.1:n.330+3821T>C (SSUH2)
XM_017006530.1:c.-283+3821T>C (SSUH2) XP_016862019.1:n.-283+3821T>C
NM_001234.5:c.114+4648A>G (CAV3) NP_001225.1:n.114+4648A>G
NM_033337.3:c.114+4648A>G (CAV3) MANE Select NP_203123.1:n.114+4648A>G