Canonical Allele Identifier: CA1344396654

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733937G= , CM000665.2:g.8733937G= GRCh38
NC_000003.11:g.8775623G= , CM000665.1:g.8775623G= GRCh37
NC_000003.10:g.8750623G= NCBI36
NG_008797.2:g.5128G= , LRG_329:g.5128G=

Transcript Alleles

HGVS Amino-acid change
ENST00000343849.3:c.61G= (CAV3) MANE Select ENSP00000341940.2:p.Glu21=
ENST00000343849.2:c.61G= (CAV3) ENSP00000341940.2:p.Glu21=
ENST00000397368.2:c.61G= (CAV3) ENSP00000380525.2:p.Glu21=
ENST00000435138.5:c.64+8522C= (SSUH2) ENSP00000412333.1:n.64+8522C=
ENST00000472766.1:n.102G= (CAV3)
ENST00000478513.1:n.335+8522C= (SSUH2)
NM_001234.4:c.61G= (CAV3) NP_001225.1:p.Glu21=
NM_033337.2:c.61G= , LRG_329t1:c.61G= (CAV3) NP_203123.1:p.Glu21=
XR_940435.1:n.330+8522C= (SSUH2)
XM_017006530.1:c.-283+8522C= (SSUH2) XP_016862019.1:n.-283+8522C=
NM_001234.5:c.61G= (CAV3) NP_001225.1:p.Glu21=
NM_033337.3:c.61G= (CAV3) MANE Select NP_203123.1:p.Glu21=