Canonical Allele Identifier: CA392000254
Gene: CAPN3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42402876T>A , CM000677.2:g.42402876T>A GRCh38
NC_000015.9:g.42695074T>A , CM000677.1:g.42695074T>A GRCh37
NC_000015.8:g.40482366T>A NCBI36
NG_008660.1:g.59774T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349748.8:c.1475T>A ENSP00000183936.4:p.Met492Lys
ENST00000357568.8:c.1619T>A ENSP00000350181.3:p.Met540Lys
ENST00000397163.8:c.1619T>A MANE Select ENSP00000380349.3:p.Met540Lys
ENST00000466369.5:n.2128T>A
ENST00000483208.5:n.2508T>A
ENST00000495723.1:n.2508T>A
ENST00000549793.5:n.1850T>A
ENST00000638141.2:n.1490T>A
ENST00000673646.1:c.83T>A ENSP00000501007.1:p.Met28Lys
ENST00000673705.1:c.309+3224T>A ENSP00000501021.1:n.309+3224T>A
ENST00000673813.1:n.541T>A
ENST00000318023.11:c.1475T>A ENSP00000326281.8:p.Met492Lys
ENST00000349748.7:c.1475T>A ENSP00000183936.4:p.Met492Lys
ENST00000357568.7:c.1619T>A ENSP00000350181.3:p.Met540Lys
ENST00000397163.7:c.1619T>A ENSP00000380349.3:p.Met540Lys
ENST00000397200.8:c.83T>A ENSP00000380384.4:p.Met28Lys
ENST00000567071.5:c.78T>A
ENST00000569827.5:c.83T>A ENSP00000454379.1:p.Met28Lys
NM_000070.2:c.1619T>A NP_000061.1:p.Met540Lys
NM_024344.1:c.1619T>A NP_077320.1:p.Met540Lys
NM_173087.1:c.1475T>A NP_775110.1:p.Met492Lys
NM_173088.1:c.83T>A NP_775111.1:p.Met28Lys
NM_000070.3:c.1619T>A MANE Select NP_000061.1:p.Met540Lys
NM_024344.2:c.1619T>A NP_077320.1:p.Met540Lys
NM_173087.2:c.1475T>A NP_775110.1:p.Met492Lys
NM_173088.2:c.83T>A NP_775111.1:p.Met28Lys