Canonical Allele Identifier: CA1344396382

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733857T= , CM000665.2:g.8733857T= GRCh38
NC_000003.11:g.8775543T= , CM000665.1:g.8775543T= GRCh37
NC_000003.10:g.8750543T= NCBI36
NG_008797.2:g.5048T= , LRG_329:g.5048T=

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.-20T= (CAV3) MANE Select ENSP00000341940.2:n.-20T=
ENST00000343849.2:c.-20T= (CAV3) ENSP00000341940.2:n.-20T=
ENST00000435138.5:c.64+8602A= (SSUH2) ENSP00000412333.1:n.64+8602A=
ENST00000472766.1:n.22T= (CAV3)
ENST00000478513.1:n.335+8602A= (SSUH2)
NM_001234.4:c.-20T= (CAV3) NP_001225.1:n.-20T=
NM_033337.2:c.-20T= , LRG_329t1:c.-20T= (CAV3) NP_203123.1:n.-20T=
XR_940435.1:n.330+8602A= (SSUH2)
XM_017006530.1:c.-283+8602A= (SSUH2) XP_016862019.1:n.-283+8602A=
NM_001234.5:c.-20T= (CAV3) NP_001225.1:n.-20T=
NM_033337.3:c.-20T= (CAV3) MANE Select NP_203123.1:n.-20T=