Canonical Allele Identifier: CA1344396514

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733895A= , CM000665.2:g.8733895A= GRCh38
NC_000003.11:g.8775581A= , CM000665.1:g.8775581A= GRCh37
NC_000003.10:g.8750581A= NCBI36
NG_008797.2:g.5086A= , LRG_329:g.5086A=

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.19A= (CAV3) MANE Select ENSP00000341940.2:p.Thr7=
ENST00000343849.2:c.19A= (CAV3) ENSP00000341940.2:p.Thr7=
ENST00000397368.2:c.19A= (CAV3) ENSP00000380525.2:p.Thr7=
ENST00000435138.5:c.64+8564T= (SSUH2) ENSP00000412333.1:n.64+8564T=
ENST00000472766.1:n.60A= (CAV3)
ENST00000478513.1:n.335+8564T= (SSUH2)
NM_001234.4:c.19A= (CAV3) NP_001225.1:p.Thr7=
NM_033337.2:c.19A= , LRG_329t1:c.19A= (CAV3) NP_203123.1:p.Thr7=
XR_940435.1:n.330+8564T= (SSUH2)
XM_017006530.1:c.-283+8564T= (SSUH2) XP_016862019.1:n.-283+8564T=
NM_001234.5:c.19A= (CAV3) NP_001225.1:p.Thr7=
NM_033337.3:c.19A= (CAV3) MANE Select NP_203123.1:p.Thr7=