Canonical Allele Identifier: CA2577496476

Linked Data

gnomAD v4: 3-8733870-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733870C>G , CM000665.2:g.8733870C>G GRCh38
NC_000003.11:g.8775556C>G , CM000665.1:g.8775556C>G GRCh37
NC_000003.10:g.8750556C>G NCBI36
NG_008797.2:g.5061C>G , LRG_329:g.5061C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.-7C>G (CAV3) MANE Select ENSP00000341940.2:n.-7C>G
ENST00000343849.2:c.-7C>G (CAV3) ENSP00000341940.2:n.-7C>G
ENST00000397368.2:c.-7C>G (CAV3) ENSP00000380525.2:n.-7C>G
ENST00000435138.5:c.64+8589G>C (SSUH2) ENSP00000412333.1:n.64+8589G>C
ENST00000472766.1:n.35C>G (CAV3)
ENST00000478513.1:n.335+8589G>C (SSUH2)
NM_001234.4:c.-7C>G (CAV3) NP_001225.1:n.-7C>G
NM_033337.2:c.-7C>G , LRG_329t1:c.-7C>G (CAV3) NP_203123.1:n.-7C>G
XR_940435.1:n.330+8589G>C (SSUH2)
XM_017006530.1:c.-283+8589G>C (SSUH2) XP_016862019.1:n.-283+8589G>C
NM_001234.5:c.-7C>G (CAV3) NP_001225.1:n.-7C>G
NM_033337.3:c.-7C>G (CAV3) MANE Select NP_203123.1:n.-7C>G