Canonical Allele Identifier: CA7511502

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42403779T>C , CM000677.2:g.42403779T>C	GRCh38
NC_000015.9:g.42695977T>C , CM000677.1:g.42695977T>C	GRCh37
NC_000015.8:g.40483269T>C	NCBI36
NG_008660.1:g.60677T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000070.3:c.1782+2T>C MANE Select	NP_000061.1:n.1782+2T>C
ENST00000397163.8:c.1782+2T>C MANE Select	ENSP00000380349.3:n.1782+2T>C
NM_000070.2:c.1782+2T>C	NP_000061.1:n.1782+2T>C
NM_024344.1:c.1782+2T>C	NP_077320.1:n.1782+2T>C
NM_024344.2:c.1782+2T>C	NP_077320.1:n.1782+2T>C
NM_173087.1:c.1638+2T>C	NP_775110.1:n.1638+2T>C
NM_173087.2:c.1638+2T>C	NP_775110.1:n.1638+2T>C
NM_173088.1:c.246+2T>C	NP_775111.1:n.246+2T>C
NM_173088.2:c.246+2T>C	NP_775111.1:n.246+2T>C
ENST00000318023.11:c.1638+2T>C	ENSP00000326281.8:n.1638+2T>C
ENST00000349748.7:c.1638+2T>C	ENSP00000183936.4:n.1638+2T>C
ENST00000349748.8:c.1638+2T>C	ENSP00000183936.4:n.1638+2T>C
ENST00000357568.7:c.1782+2T>C	ENSP00000350181.3:n.1782+2T>C
ENST00000357568.8:c.1782+2T>C	ENSP00000350181.3:n.1782+2T>C
ENST00000397163.7:c.1782+2T>C	ENSP00000380349.3:n.1782+2T>C
ENST00000397200.8:c.246+2T>C	ENSP00000380384.4:n.246+2T>C
ENST00000466369.5:n.2291+2T>C
ENST00000483208.5:n.2673T>C
ENST00000495723.1:n.2671+2T>C
ENST00000549793.5:n.2013+2T>C
ENST00000567071.5:c.241+2T>C
ENST00000569827.5:c.246+2T>C	ENSP00000454379.1:n.246+2T>C
ENST00000638141.2:n.1653+2T>C
ENST00000673646.1:c.246+2T>C	ENSP00000501007.1:n.246+2T>C
ENST00000673705.1:c.309+4127T>C	ENSP00000501021.1:n.309+4127T>C
ENST00000673813.1:n.619T>C