Canonical Allele Identifier: CA391998767

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42684852C>T (hg19) ; chr15:g.42392654C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42392654C>T , CM000677.2:g.42392654C>T	GRCh38
NC_000015.9:g.42684852C>T , CM000677.1:g.42684852C>T	GRCh37
NC_000015.8:g.40472144C>T	NCBI36
NG_008660.1:g.49552C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.817C>T	ENSP00000183936.4:p.Gln273Ter
ENST00000357568.8:c.961C>T	ENSP00000350181.3:p.Gln321Ter
ENST00000397163.8:c.961C>T MANE Select	ENSP00000380349.3:p.Gln321Ter
ENST00000466369.5:n.1470C>T
ENST00000483208.5:n.1192C>T
ENST00000495723.1:n.1192C>T
ENST00000549793.5:n.1192C>T
ENST00000638141.2:n.832C>T
ENST00000673705.1:c.71-4146C>T	ENSP00000501021.1:n.71-4146C>T
ENST00000318023.11:c.817C>T	ENSP00000326281.8:p.Gln273Ter
ENST00000349748.7:c.817C>T	ENSP00000183936.4:p.Gln273Ter
ENST00000357568.7:c.961C>T	ENSP00000350181.3:p.Gln321Ter
ENST00000397163.7:c.961C>T	ENSP00000380349.3:p.Gln321Ter
NM_000070.2:c.961C>T	NP_000061.1:p.Gln321Ter
NM_024344.1:c.961C>T	NP_077320.1:p.Gln321Ter
NM_173087.1:c.817C>T	NP_775110.1:p.Gln273Ter
NM_000070.3:c.961C>T MANE Select	NP_000061.1:p.Gln321Ter
NM_024344.2:c.961C>T	NP_077320.1:p.Gln321Ter
NM_173087.2:c.817C>T	NP_775110.1:p.Gln273Ter