Canonical Allele Identifier: CA391998408

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42681292G>T (hg19) ; chr15:g.42389094G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42389094G>T , CM000677.2:g.42389094G>T	GRCh38
NC_000015.9:g.42681292G>T , CM000677.1:g.42681292G>T	GRCh37
NC_000015.8:g.40468584G>T	NCBI36
NG_008660.1:g.45992G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.799G>T	ENSP00000183936.4:p.Asp267Tyr
ENST00000357568.8:c.799G>T	ENSP00000350181.3:p.Asp267Tyr
ENST00000397163.8:c.799G>T MANE Select	ENSP00000380349.3:p.Asp267Tyr
ENST00000466369.5:n.1308G>T
ENST00000483208.5:n.1030G>T
ENST00000495723.1:n.1030G>T
ENST00000549793.5:n.1030G>T
ENST00000638141.2:n.814G>T
ENST00000673705.1:c.70+4542G>T	ENSP00000501021.1:n.70+4542G>T
ENST00000318023.11:c.799G>T	ENSP00000326281.8:p.Asp267Tyr
ENST00000349748.7:c.799G>T	ENSP00000183936.4:p.Asp267Tyr
ENST00000357568.7:c.799G>T	ENSP00000350181.3:p.Asp267Tyr
ENST00000397163.7:c.799G>T	ENSP00000380349.3:p.Asp267Tyr
NM_000070.2:c.799G>T	NP_000061.1:p.Asp267Tyr
NM_024344.1:c.799G>T	NP_077320.1:p.Asp267Tyr
NM_173087.1:c.799G>T	NP_775110.1:p.Asp267Tyr
NM_000070.3:c.799G>T MANE Select	NP_000061.1:p.Asp267Tyr
NM_024344.2:c.799G>T	NP_077320.1:p.Asp267Tyr
NM_173087.2:c.799G>T	NP_775110.1:p.Asp267Tyr