Canonical Allele Identifier: CA2803911722

Gene: CAPN3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42410171G>T , CM000677.2:g.42410171G>T	GRCh38
NC_000015.9:g.42702369G>T , CM000677.1:g.42702369G>T	GRCh37
NC_000015.8:g.40489661G>T	NCBI36
NG_008660.1:g.67069G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337571.9:c.120+176G>T	ENSP00000336840.4:n.120+176G>T
ENST00000349748.8:c.1839+176G>T	ENSP00000183936.4:n.1839+176G>T
ENST00000357568.8:c.2097+176G>T	ENSP00000350181.3:n.2097+176G>T
ENST00000397163.8:c.2115+176G>T MANE Select	ENSP00000380349.3:n.2115+176G>T
ENST00000397204.9:c.120+176G>T	ENSP00000380387.4:n.120+176G>T
ENST00000466222.7:n.380+176G>T
ENST00000466369.5:n.2606+176G>T
ENST00000495723.1:n.2986+176G>T
ENST00000549793.5:n.2328+176G>T
ENST00000562199.2:c.123+176G>T	ENSP00000501034.1:n.123+176G>T
ENST00000569136.6:c.120+176G>T	ENSP00000455254.1:n.120+176G>T
ENST00000638141.2:n.1854+176G>T
ENST00000673646.1:c.679+176G>T	ENSP00000501007.1:n.679+176G>T
ENST00000673687.1:n.368G>T
ENST00000673692.1:c.120+176G>T	ENSP00000501138.1:n.120+176G>T
ENST00000673705.1:c.510+176G>T	ENSP00000501021.1:n.510+176G>T
ENST00000673743.1:c.18+176G>T	ENSP00000500989.1:n.18+176G>T
ENST00000673750.1:c.120+176G>T	ENSP00000501173.1:n.120+176G>T
ENST00000673771.1:c.120+176G>T	ENSP00000501023.1:n.120+176G>T
ENST00000673774.1:n.992G>T
ENST00000673839.1:c.120+176G>T	ENSP00000501188.1:n.120+176G>T
ENST00000673851.1:c.120+176G>T	ENSP00000501142.1:n.120+176G>T
ENST00000673854.1:n.5537+176G>T
ENST00000673886.1:c.120+176G>T	ENSP00000501155.1:n.120+176G>T
ENST00000673890.1:c.120+176G>T	ENSP00000501293.1:n.120+176G>T
ENST00000673893.1:c.215G>T	ENSP00000500987.1:n.215G>T
ENST00000673928.1:c.120+176G>T	ENSP00000501099.1:n.120+176G>T
ENST00000673936.1:c.120+176G>T	ENSP00000501189.1:n.120+176G>T
ENST00000673939.1:c.120+176G>T	ENSP00000501129.1:n.120+176G>T
ENST00000673950.1:n.389+176G>T
ENST00000673978.1:c.258+176G>T	ENSP00000500976.1:n.258+176G>T
ENST00000673987.1:c.120+176G>T	ENSP00000501231.1:n.120+176G>T
ENST00000674011.1:c.120+176G>T	ENSP00000501171.1:n.120+176G>T
ENST00000674018.1:c.120+176G>T	ENSP00000501271.1:n.120+176G>T
ENST00000674027.1:n.175+176G>T
ENST00000674041.1:c.120+176G>T	ENSP00000500956.1:n.120+176G>T
ENST00000674052.1:c.339+176G>T	ENSP00000501057.1:n.339+176G>T
ENST00000674093.1:c.120+176G>T	ENSP00000501303.1:n.120+176G>T
ENST00000674119.1:c.120+176G>T	ENSP00000501217.1:n.120+176G>T
ENST00000674130.1:n.509G>T
ENST00000674135.1:c.297+176G>T	ENSP00000501178.1:n.297+176G>T
ENST00000674139.1:c.120+176G>T	ENSP00000501054.1:n.120+176G>T
ENST00000674146.1:c.120+176G>T	ENSP00000501175.1:n.120+176G>T
ENST00000674149.1:c.120+176G>T	ENSP00000501112.1:n.120+176G>T
ENST00000318023.11:c.1971+176G>T	ENSP00000326281.8:n.1971+176G>T
ENST00000337571.8:c.120+176G>T	ENSP00000336840.4:n.120+176G>T
ENST00000349748.7:c.1839+176G>T	ENSP00000183936.4:n.1839+176G>T
ENST00000356316.7:c.120+176G>T	ENSP00000348667.4:n.120+176G>T
ENST00000357568.7:c.2097+176G>T	ENSP00000350181.3:n.2097+176G>T
ENST00000397163.7:c.2115+176G>T	ENSP00000380349.3:n.2115+176G>T
ENST00000397200.8:c.579+176G>T	ENSP00000380384.4:n.579+176G>T
ENST00000397204.8:c.120+176G>T	ENSP00000380387.4:n.120+176G>T
ENST00000466222.6:n.1038+176G>T
ENST00000561817.5:c.120+176G>T	ENSP00000456575.1:n.120+176G>T
ENST00000562199.1:n.123+176G>T
ENST00000564503.5:c.212+176G>T
ENST00000565274.5:c.327+176G>T	ENSP00000457759.1:n.327+176G>T
ENST00000565559.5:c.297+176G>T	ENSP00000457878.1:n.297+176G>T
ENST00000569136.5:c.120+176G>T	ENSP00000455254.1:n.120+176G>T
ENST00000569827.5:c.447+176G>T	ENSP00000454379.1:n.447+176G>T
NM_000070.2:c.2115+176G>T	NP_000061.1:n.2115+176G>T
NM_024344.1:c.2097+176G>T	NP_077320.1:n.2097+176G>T
NM_173087.1:c.1839+176G>T	NP_775110.1:n.1839+176G>T
NM_173088.1:c.579+176G>T	NP_775111.1:n.579+176G>T
NM_173089.1:c.120+176G>T	NP_775112.1:n.120+176G>T
NM_173090.1:c.120+176G>T	NP_775113.1:n.120+176G>T
NM_000070.3:c.2115+176G>T MANE Select	NP_000061.1:n.2115+176G>T
NM_024344.2:c.2097+176G>T	NP_077320.1:n.2097+176G>T
NM_173087.2:c.1839+176G>T	NP_775110.1:n.1839+176G>T
NM_173088.2:c.579+176G>T	NP_775111.1:n.579+176G>T
NM_173089.2:c.120+176G>T	NP_775112.1:n.120+176G>T
NM_173090.2:c.120+176G>T	NP_775113.1:n.120+176G>T