Canonical Allele Identifier: CA489999209

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 2018320
• ClinVar RCV Id: RCV002861941
• dbSNP Id: rs1421130687
• MyVariant Identifiers: chr15:g.42652246A>G (hg19) ; chr15:g.42360048A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42360048A>G , CM000677.2:g.42360048A>G	GRCh38
NC_000015.9:g.42652246A>G , CM000677.1:g.42652246A>G	GRCh37
NC_000015.8:g.40439538A>G	NCBI36
NG_008660.1:g.16946A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.243A>G	ENSP00000183936.4:p.Pro81=
ENST00000357568.8:c.243A>G	ENSP00000350181.3:p.Pro81=
ENST00000397163.8:c.243A>G MANE Select	ENSP00000380349.3:p.Pro81=
ENST00000466369.5:n.540+5595A>G
ENST00000483208.5:n.540+5595A>G
ENST00000495723.1:n.540+5595A>G
ENST00000549793.5:n.540+5595A>G
ENST00000318023.11:c.243A>G	ENSP00000326281.8:p.Pro81=
ENST00000349748.7:c.243A>G	ENSP00000183936.4:p.Pro81=
ENST00000357568.7:c.243A>G	ENSP00000350181.3:p.Pro81=
ENST00000397163.7:c.243A>G	ENSP00000380349.3:p.Pro81=
NM_000070.2:c.243A>G	NP_000061.1:p.Pro81=
NM_024344.1:c.243A>G	NP_077320.1:p.Pro81=
NM_173087.1:c.243A>G	NP_775110.1:p.Pro81=
NM_000070.3:c.243A>G MANE Select	NP_000061.1:p.Pro81=
NM_024344.2:c.243A>G	NP_077320.1:p.Pro81=
NM_173087.2:c.243A>G	NP_775110.1:p.Pro81=