Canonical Allele Identifier: CA2236268

Linked Data

ClinVar Variation Id: 1292446
ClinVar RCV Id: RCV001714454
dbSNP Id: rs368151958
gnomAD v2: 3-8775517-G-A
gnomAD v3: 3-8733831-G-A
gnomAD v4: 3-8733831-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733831G>A , CM000665.2:g.8733831G>A GRCh38
NC_000003.11:g.8775517G>A , CM000665.1:g.8775517G>A GRCh37
NC_000003.10:g.8750517G>A NCBI36
NG_008797.2:g.5022G>A , LRG_329:g.5022G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.-46G>A (CAV3) MANE Select ENSP00000341940.2:n.-46G>A
ENST00000343849.2:c.-46G>A (CAV3) ENSP00000341940.2:n.-46G>A
ENST00000435138.5:c.64+8628C>T (SSUH2) ENSP00000412333.1:n.64+8628C>T
ENST00000478513.1:n.335+8628C>T (SSUH2)
NM_001234.4:c.-46G>A (CAV3) NP_001225.1:n.-46G>A
NM_033337.2:c.-46G>A , LRG_329t1:c.-46G>A (CAV3) NP_203123.1:n.-46G>A
XR_940435.1:n.330+8628C>T (SSUH2)
XM_017006530.1:c.-283+8628C>T (SSUH2) XP_016862019.1:n.-283+8628C>T
NM_001234.5:c.-46G>A (CAV3) NP_001225.1:n.-46G>A
NM_033337.3:c.-46G>A (CAV3) MANE Select NP_203123.1:n.-46G>A