Canonical Allele Identifier: CA2803913501
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42389174_42389175insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC , CM000677.2:g.42389174_42389175insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC GRCh38
NC_000015.9:g.42681372_42681373insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC , CM000677.1:g.42681372_42681373insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC GRCh37
NC_000015.8:g.40468664_40468665insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC NCBI36
NG_008660.1:g.46072_46073insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC ENSP00000183936.4:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGAC...
ENST00000357568.8:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC ENSP00000350181.3:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGAC...
ENST00000397163.8:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC MANE Select ENSP00000380349.3:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGAC...
ENST00000466369.5:n.1310+78_1310+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC
ENST00000483208.5:n.1032+78_1032+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC
ENST00000495723.1:n.1032+78_1032+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC
ENST00000549793.5:n.1032+78_1032+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC
ENST00000638141.2:n.816+78_816+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC
ENST00000673705.1:c.70+4622_70+4623insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC ENSP00000501021.1:n.70+4622_70+4623insTAGGGTCGCGGCGAATCACGCCG...
ENST00000318023.11:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC ENSP00000326281.8:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGAC...
ENST00000349748.7:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC ENSP00000183936.4:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGAC...
ENST00000357568.7:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC ENSP00000350181.3:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGAC...
ENST00000397163.7:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC ENSP00000380349.3:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGAC...
NM_000070.2:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC NP_000061.1:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCC...
NM_024344.1:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC NP_077320.1:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCC...
NM_173087.1:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC NP_775110.1:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCC...
NM_000070.3:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC MANE Select NP_000061.1:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCC...
NM_024344.2:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC NP_077320.1:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCC...
NM_173087.2:c.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCCCTTAGCAGCC NP_775110.1:n.801+78_801+79insTAGGGTCGCGGCGAATCACGCCGACAGCGCC...