Canonical Allele Identifier: CA2172714540
Gene: CAPN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42402897_42402898delinsTC , CM000677.2:g.42402897_42402898delinsTC GRCh38
NC_000015.9:g.42695095_42695096delinsTC , CM000677.1:g.42695095_42695096delinsTC GRCh37
NC_000015.8:g.40482387_40482388delinsTC NCBI36
NG_008660.1:g.59795_59796delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.1496_1497delinsTC ENSP00000183936.4:p.Phe499=
ENST00000357568.8:c.1640_1641delinsTC ENSP00000350181.3:p.Phe547=
ENST00000397163.8:c.1640_1641delinsTC MANE Select ENSP00000380349.3:p.Phe547=
ENST00000466369.5:n.2149_2150delinsTC
ENST00000483208.5:n.2529_2530delinsTC
ENST00000495723.1:n.2529_2530delinsTC
ENST00000549793.5:n.1871_1872delinsTC
ENST00000638141.2:n.1511_1512delinsTC
ENST00000673646.1:c.104_105delinsTC ENSP00000501007.1:p.Phe35=
ENST00000673705.1:c.309+3245_309+3246delinsTC ENSP00000501021.1:n.309+3245_309+3246delinsTC
ENST00000673813.1:n.562_563delinsTC
ENST00000318023.11:c.1496_1497delinsTC ENSP00000326281.8:p.Phe499=
ENST00000349748.7:c.1496_1497delinsTC ENSP00000183936.4:p.Phe499=
ENST00000357568.7:c.1640_1641delinsTC ENSP00000350181.3:p.Phe547=
ENST00000397163.7:c.1640_1641delinsTC ENSP00000380349.3:p.Phe547=
ENST00000397200.8:c.104_105delinsTC ENSP00000380384.4:p.Phe35=
ENST00000567071.5:c.99_100delinsTC
ENST00000569827.5:c.104_105delinsTC ENSP00000454379.1:p.Phe35=
NM_000070.2:c.1640_1641delinsTC NP_000061.1:p.Phe547=
NM_024344.1:c.1640_1641delinsTC NP_077320.1:p.Phe547=
NM_173087.1:c.1496_1497delinsTC NP_775110.1:p.Phe499=
NM_173088.1:c.104_105delinsTC NP_775111.1:p.Phe35=
NM_000070.3:c.1640_1641delinsTC MANE Select NP_000061.1:p.Phe547=
NM_024344.2:c.1640_1641delinsTC NP_077320.1:p.Phe547=
NM_173087.2:c.1496_1497delinsTC NP_775110.1:p.Phe499=
NM_173088.2:c.104_105delinsTC NP_775111.1:p.Phe35=