Canonical Allele Identifier: CA1344396381

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733856G= , CM000665.2:g.8733856G= GRCh38
NC_000003.11:g.8775542G= , CM000665.1:g.8775542G= GRCh37
NC_000003.10:g.8750542G= NCBI36
NG_008797.2:g.5047G= , LRG_329:g.5047G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343849.3:c.-21G= (CAV3) MANE Select ENSP00000341940.2:n.-21G=
ENST00000343849.2:c.-21G= (CAV3) ENSP00000341940.2:n.-21G=
ENST00000435138.5:c.64+8603C= (SSUH2) ENSP00000412333.1:n.64+8603C=
ENST00000472766.1:n.21G= (CAV3)
ENST00000478513.1:n.335+8603C= (SSUH2)
NM_001234.4:c.-21G= (CAV3) NP_001225.1:n.-21G=
NM_033337.2:c.-21G= , LRG_329t1:c.-21G= (CAV3) NP_203123.1:n.-21G=
XR_940435.1:n.330+8603C= (SSUH2)
XM_017006530.1:c.-283+8603C= (SSUH2) XP_016862019.1:n.-283+8603C=
NM_001234.5:c.-21G= (CAV3) NP_001225.1:n.-21G=
NM_033337.3:c.-21G= (CAV3) MANE Select NP_203123.1:n.-21G=