Canonical Allele Identifier: CA392002287

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42703511G>T (hg19) ; chr15:g.42411313G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42411313G>T , CM000677.2:g.42411313G>T	GRCh38
NC_000015.9:g.42703511G>T , CM000677.1:g.42703511G>T	GRCh37
NC_000015.8:g.40490803G>T	NCBI36
NG_008660.1:g.68211G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000337571.9:c.412G>T	ENSP00000336840.4:p.Gly138Ter
ENST00000349748.8:c.2131G>T	ENSP00000183936.4:p.Gly711Ter
ENST00000357568.8:c.2389G>T	ENSP00000350181.3:p.Gly797Ter
ENST00000397163.8:c.2407G>T MANE Select	ENSP00000380349.3:p.Gly803Ter
ENST00000397204.9:c.412G>T	ENSP00000380387.4:p.Gly138Ter
ENST00000466222.7:n.778G>T
ENST00000466369.5:n.2898G>T
ENST00000495723.1:n.3278G>T
ENST00000549793.5:n.2620G>T
ENST00000562199.2:c.411G>T	ENSP00000501034.1:n.411G>T
ENST00000567817.6:c.196G>T	ENSP00000456514.2:p.Gly66Ter
ENST00000568153.2:c.273G>T
ENST00000569136.6:c.412G>T	ENSP00000455254.1:p.Gly138Ter
ENST00000638141.2:n.2146G>T
ENST00000673646.1:c.971G>T	ENSP00000501007.1:n.971G>T
ENST00000673684.1:n.389G>T
ENST00000673692.1:c.412G>T	ENSP00000501138.1:p.Gly138Ter
ENST00000673705.1:c.1236G>T	ENSP00000501021.1:n.1236G>T
ENST00000673743.1:c.310G>T	ENSP00000500989.1:p.Gly104Ter
ENST00000673750.1:c.412G>T	ENSP00000501173.1:p.Gly138Ter
ENST00000673771.1:c.412G>T	ENSP00000501023.1:p.Gly138Ter
ENST00000673774.1:n.1540G>T
ENST00000673839.1:c.412G>T	ENSP00000501188.1:p.Gly138Ter
ENST00000673851.1:c.412G>T	ENSP00000501142.1:p.Gly138Ter
ENST00000673854.1:n.5829G>T
ENST00000673886.1:c.412G>T	ENSP00000501155.1:p.Gly138Ter
ENST00000673890.1:c.412G>T	ENSP00000501293.1:p.Gly138Ter
ENST00000673928.1:c.412G>T	ENSP00000501099.1:p.Gly138Ter
ENST00000673936.1:c.412G>T	ENSP00000501189.1:p.Gly138Ter
ENST00000673939.1:c.*127G>T	ENSP00000501129.1:n.*127G>T
ENST00000673950.1:n.681G>T
ENST00000673978.1:c.550G>T	ENSP00000500976.1:p.Gly184Ter
ENST00000673987.1:c.*127G>T	ENSP00000501231.1:n.*127G>T
ENST00000674011.1:c.*201G>T	ENSP00000501171.1:n.*201G>T
ENST00000674018.1:c.412G>T	ENSP00000501271.1:p.Gly138Ter
ENST00000674027.1:n.558G>T
ENST00000674041.1:c.412G>T	ENSP00000500956.1:p.Gly138Ter
ENST00000674052.1:c.631G>T	ENSP00000501057.1:p.Gly211Ter
ENST00000674093.1:c.412G>T	ENSP00000501303.1:p.Gly138Ter
ENST00000674119.1:c.412G>T	ENSP00000501217.1:p.Gly138Ter
ENST00000674135.1:c.589G>T	ENSP00000501178.1:p.Gly197Ter
ENST00000674139.1:c.412G>T	ENSP00000501054.1:p.Gly138Ter
ENST00000674146.1:c.412G>T	ENSP00000501175.1:p.Gly138Ter
ENST00000674149.1:c.412G>T	ENSP00000501112.1:p.Gly138Ter
ENST00000318023.11:c.2263G>T	ENSP00000326281.8:p.Gly755Ter
ENST00000337571.8:c.412G>T	ENSP00000336840.4:p.Gly138Ter
ENST00000349748.7:c.2131G>T	ENSP00000183936.4:p.Gly711Ter
ENST00000356316.7:c.412G>T	ENSP00000348667.4:p.Gly138Ter
ENST00000357568.7:c.2389G>T	ENSP00000350181.3:p.Gly797Ter
ENST00000397163.7:c.2407G>T	ENSP00000380349.3:p.Gly803Ter
ENST00000397200.8:c.871G>T	ENSP00000380384.4:p.Gly291Ter
ENST00000397204.8:c.412G>T	ENSP00000380387.4:p.Gly138Ter
ENST00000466222.6:n.1330G>T
ENST00000561817.5:c.412G>T	ENSP00000456575.1:p.Gly138Ter
ENST00000564503.5:c.450G>T
ENST00000565274.5:c.585G>T	ENSP00000457759.1:n.585G>T
ENST00000567817.5:c.223G>T	ENSP00000456514.1:p.Gly75Ter
ENST00000568153.1:c.144G>T
ENST00000569136.5:c.412G>T	ENSP00000455254.1:p.Gly138Ter
ENST00000569827.5:c.739G>T	ENSP00000454379.1:p.Gly247Ter
NM_000070.2:c.2407G>T	NP_000061.1:p.Gly803Ter
NM_024344.1:c.2389G>T	NP_077320.1:p.Gly797Ter
NM_173087.1:c.2131G>T	NP_775110.1:p.Gly711Ter
NM_173088.1:c.871G>T	NP_775111.1:p.Gly291Ter
NM_173089.1:c.412G>T	NP_775112.1:p.Gly138Ter
NM_173090.1:c.412G>T	NP_775113.1:p.Gly138Ter
NM_000070.3:c.2407G>T MANE Select	NP_000061.1:p.Gly803Ter
NM_024344.2:c.2389G>T	NP_077320.1:p.Gly797Ter
NM_173087.2:c.2131G>T	NP_775110.1:p.Gly711Ter
NM_173088.2:c.871G>T	NP_775111.1:p.Gly291Ter
NM_173089.2:c.412G>T	NP_775112.1:p.Gly138Ter
NM_173090.2:c.412G>T	NP_775113.1:p.Gly138Ter