Canonical Allele Identifier: CA489885771

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42702139G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42409941G>T , CM000677.2:g.42409941G>T	GRCh38
NC_000015.9:g.42702139G>T , CM000677.1:g.42702139G>T	GRCh37
NC_000015.8:g.40489431G>T	NCBI36
NG_008660.1:g.66839G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337571.9:c.66G>T	ENSP00000336840.4:p.Leu22=
ENST00000349748.8:c.1785G>T	ENSP00000183936.4:p.Leu595=
ENST00000357568.8:c.2043G>T	ENSP00000350181.3:p.Leu681=
ENST00000397163.8:c.2061G>T MANE Select	ENSP00000380349.3:p.Leu687=
ENST00000397204.9:c.66G>T	ENSP00000380387.4:p.Leu22=
ENST00000466222.7:n.326G>T
ENST00000466369.5:n.2552G>T
ENST00000495723.1:n.2932G>T
ENST00000549793.5:n.2274G>T
ENST00000562199.2:c.69G>T	ENSP00000501034.1:p.Leu23=
ENST00000569136.6:c.66G>T	ENSP00000455254.1:p.Leu22=
ENST00000638141.2:n.1800G>T
ENST00000673646.1:c.625G>T	ENSP00000501007.1:n.625G>T
ENST00000673687.1:n.138G>T
ENST00000673692.1:c.66G>T	ENSP00000501138.1:p.Leu22=
ENST00000673705.1:c.456G>T	ENSP00000501021.1:n.456G>T
ENST00000673743.1:c.-37G>T	ENSP00000500989.1:n.-37G>T
ENST00000673750.1:c.66G>T	ENSP00000501173.1:p.Leu22=
ENST00000673771.1:c.66G>T	ENSP00000501023.1:p.Leu22=
ENST00000673774.1:n.762G>T
ENST00000673839.1:c.66G>T	ENSP00000501188.1:p.Leu22=
ENST00000673851.1:c.66G>T	ENSP00000501142.1:p.Leu22=
ENST00000673854.1:n.5483G>T
ENST00000673886.1:c.66G>T	ENSP00000501155.1:p.Leu22=
ENST00000673890.1:c.66G>T	ENSP00000501293.1:p.Leu22=
ENST00000673928.1:c.66G>T	ENSP00000501099.1:p.Leu22=
ENST00000673936.1:c.66G>T	ENSP00000501189.1:p.Leu22=
ENST00000673939.1:c.66G>T	ENSP00000501129.1:p.Leu22=
ENST00000673950.1:n.335G>T
ENST00000673978.1:c.204G>T	ENSP00000500976.1:p.Leu68=
ENST00000673987.1:c.66G>T	ENSP00000501231.1:p.Leu22=
ENST00000674011.1:c.66G>T	ENSP00000501171.1:p.Leu22=
ENST00000674018.1:c.66G>T	ENSP00000501271.1:p.Leu22=
ENST00000674027.1:n.121G>T
ENST00000674041.1:c.66G>T	ENSP00000500956.1:p.Leu22=
ENST00000674052.1:c.285G>T	ENSP00000501057.1:p.Leu95=
ENST00000674093.1:c.66G>T	ENSP00000501303.1:p.Leu22=
ENST00000674119.1:c.66G>T	ENSP00000501217.1:p.Leu22=
ENST00000674130.1:n.279G>T
ENST00000674135.1:c.243G>T	ENSP00000501178.1:p.Leu81=
ENST00000674139.1:c.66G>T	ENSP00000501054.1:p.Leu22=
ENST00000674146.1:c.66G>T	ENSP00000501175.1:p.Leu22=
ENST00000674149.1:c.66G>T	ENSP00000501112.1:p.Leu22=
ENST00000318023.11:c.1917G>T	ENSP00000326281.8:p.Leu639=
ENST00000337571.8:c.66G>T	ENSP00000336840.4:p.Leu22=
ENST00000349748.7:c.1785G>T	ENSP00000183936.4:p.Leu595=
ENST00000356316.7:c.66G>T	ENSP00000348667.4:p.Leu22=
ENST00000357568.7:c.2043G>T	ENSP00000350181.3:p.Leu681=
ENST00000397163.7:c.2061G>T	ENSP00000380349.3:p.Leu687=
ENST00000397200.8:c.525G>T	ENSP00000380384.4:p.Leu175=
ENST00000397204.8:c.66G>T	ENSP00000380387.4:p.Leu22=
ENST00000466222.6:n.984G>T
ENST00000561817.5:c.66G>T	ENSP00000456575.1:p.Leu22=
ENST00000562199.1:n.69G>T
ENST00000564503.5:c.158G>T
ENST00000565274.5:c.273G>T	ENSP00000457759.1:p.Leu91=
ENST00000565559.5:c.243G>T	ENSP00000457878.1:p.Leu81=
ENST00000567071.5:c.541G>T
ENST00000569136.5:c.66G>T	ENSP00000455254.1:p.Leu22=
ENST00000569827.5:c.393G>T	ENSP00000454379.1:p.Leu131=
NM_000070.2:c.2061G>T	NP_000061.1:p.Leu687=
NM_024344.1:c.2043G>T	NP_077320.1:p.Leu681=
NM_173087.1:c.1785G>T	NP_775110.1:p.Leu595=
NM_173088.1:c.525G>T	NP_775111.1:p.Leu175=
NM_173089.1:c.66G>T	NP_775112.1:p.Leu22=
NM_173090.1:c.66G>T	NP_775113.1:p.Leu22=
NM_000070.3:c.2061G>T MANE Select	NP_000061.1:p.Leu687=
NM_024344.2:c.2043G>T	NP_077320.1:p.Leu681=
NM_173087.2:c.1785G>T	NP_775110.1:p.Leu595=
NM_173088.2:c.525G>T	NP_775111.1:p.Leu175=
NM_173089.2:c.66G>T	NP_775112.1:p.Leu22=
NM_173090.2:c.66G>T	NP_775113.1:p.Leu22=