Canonical Allele Identifier: CA391998188

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 1701252
• ClinVar RCV Id: RCV002276009
• dbSNP Id: rs886042440
• MyVariant Identifiers: chr15:g.42681193G>T (hg19) ; chr15:g.42388995G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42388995G>T , CM000677.2:g.42388995G>T	GRCh38
NC_000015.9:g.42681193G>T , CM000677.1:g.42681193G>T	GRCh37
NC_000015.8:g.40468485G>T	NCBI36
NG_008660.1:g.45893G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.700G>T	ENSP00000183936.4:p.Gly234Trp
ENST00000357568.8:c.700G>T	ENSP00000350181.3:p.Gly234Trp
ENST00000397163.8:c.700G>T MANE Select	ENSP00000380349.3:p.Gly234Trp
ENST00000466369.5:n.1209G>T
ENST00000483208.5:n.931G>T
ENST00000495723.1:n.931G>T
ENST00000549793.5:n.931G>T
ENST00000638141.2:n.715G>T
ENST00000673705.1:c.70+4443G>T	ENSP00000501021.1:n.70+4443G>T
ENST00000318023.11:c.700G>T	ENSP00000326281.8:p.Gly234Trp
ENST00000349748.7:c.700G>T	ENSP00000183936.4:p.Gly234Trp
ENST00000357568.7:c.700G>T	ENSP00000350181.3:p.Gly234Trp
ENST00000397163.7:c.700G>T	ENSP00000380349.3:p.Gly234Trp
NM_000070.2:c.700G>T	NP_000061.1:p.Gly234Trp
NM_024344.1:c.700G>T	NP_077320.1:p.Gly234Trp
NM_173087.1:c.700G>T	NP_775110.1:p.Gly234Trp
NM_000070.3:c.700G>T MANE Select	NP_000061.1:p.Gly234Trp
NM_024344.2:c.700G>T	NP_077320.1:p.Gly234Trp
NM_173087.2:c.700G>T	NP_775110.1:p.Gly234Trp