Canonical Allele Identifier: CA1344397631

Linked Data

dbSNP Id: rs1707677486

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8734386_8734394del , CM000665.2:g.8734386_8734394del GRCh38
NC_000003.11:g.8776072_8776080del , CM000665.1:g.8776072_8776080del GRCh37
NC_000003.10:g.8751072_8751080del NCBI36
NG_008797.2:g.5577_5585del , LRG_329:g.5577_5585del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343849.3:c.114+396_114+404del (CAV3) MANE Select ENSP00000341940.2:n.114+396_114+404del
ENST00000343849.2:c.114+396_114+404del (CAV3) ENSP00000341940.2:n.114+396_114+404del
ENST00000397368.2:c.114+396_114+404del (CAV3) ENSP00000380525.2:n.114+396_114+404del
ENST00000435138.5:c.64+8068_64+8076del (SSUH2) ENSP00000412333.1:n.64+8068_64+8076del
ENST00000472766.1:n.155+396_155+404del (CAV3)
ENST00000478513.1:n.335+8068_335+8076del (SSUH2)
NM_001234.4:c.114+396_114+404del (CAV3) NP_001225.1:n.114+396_114+404del
NM_033337.2:c.114+396_114+404del , LRG_329t1:c.114+396_114+404del (CAV3) NP_203123.1:n.114+396_114+404del
XR_940435.1:n.330+8068_330+8076del (SSUH2)
XM_017006530.1:c.-283+8068_-283+8076del (SSUH2) XP_016862019.1:n.-283+8068_-283+8076del
NM_001234.5:c.114+396_114+404del (CAV3) NP_001225.1:n.114+396_114+404del
NM_033337.3:c.114+396_114+404del (CAV3) MANE Select NP_203123.1:n.114+396_114+404del