Canonical Allele Identifier: CA1344403983

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8741852C= , CM000665.2:g.8741852C= GRCh38
NC_000003.11:g.8783538C= , CM000665.1:g.8783538C= GRCh37
NC_000003.10:g.8758538C= NCBI36
NG_008797.2:g.13043C= , LRG_329:g.13043C=

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.115-3674C= (CAV3) MANE Select ENSP00000341940.2:n.115-3674C=
ENST00000343849.2:c.115-3674C= (CAV3) ENSP00000341940.2:n.115-3674C=
ENST00000397368.2:c.115-3674C= (CAV3) ENSP00000380525.2:n.115-3674C=
ENST00000435138.5:c.64+607G= (SSUH2) ENSP00000412333.1:n.64+607G=
ENST00000472766.1:n.155+7862C= (CAV3)
ENST00000478513.1:n.335+607G= (SSUH2)
NM_001234.4:c.115-3674C= (CAV3) NP_001225.1:n.115-3674C=
NM_033337.2:c.115-3674C= , LRG_329t1:c.115-3674C= (CAV3) NP_203123.1:n.115-3674C=
XR_940435.1:n.330+607G= (SSUH2)
XM_017006530.1:c.-283+607G= (SSUH2) XP_016862019.1:n.-283+607G=
NM_001234.5:c.115-3674C= (CAV3) NP_001225.1:n.115-3674C=
NM_033337.3:c.115-3674C= (CAV3) MANE Select NP_203123.1:n.115-3674C=