Canonical Allele Identifier: CA489885780

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42702151G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42409953G>T , CM000677.2:g.42409953G>T	GRCh38
NC_000015.9:g.42702151G>T , CM000677.1:g.42702151G>T	GRCh37
NC_000015.8:g.40489443G>T	NCBI36
NG_008660.1:g.66851G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337571.9:c.78G>T	ENSP00000336840.4:p.Gly26=
ENST00000349748.8:c.1797G>T	ENSP00000183936.4:p.Gly599=
ENST00000357568.8:c.2055G>T	ENSP00000350181.3:p.Gly685=
ENST00000397163.8:c.2073G>T MANE Select	ENSP00000380349.3:p.Gly691=
ENST00000397204.9:c.78G>T	ENSP00000380387.4:p.Gly26=
ENST00000466222.7:n.338G>T
ENST00000466369.5:n.2564G>T
ENST00000495723.1:n.2944G>T
ENST00000549793.5:n.2286G>T
ENST00000562199.2:c.81G>T	ENSP00000501034.1:p.Gly27=
ENST00000569136.6:c.78G>T	ENSP00000455254.1:p.Gly26=
ENST00000638141.2:n.1812G>T
ENST00000673646.1:c.637G>T	ENSP00000501007.1:n.637G>T
ENST00000673687.1:n.150G>T
ENST00000673692.1:c.78G>T	ENSP00000501138.1:p.Gly26=
ENST00000673705.1:c.468G>T	ENSP00000501021.1:n.468G>T
ENST00000673743.1:c.-25G>T	ENSP00000500989.1:n.-25G>T
ENST00000673750.1:c.78G>T	ENSP00000501173.1:p.Gly26=
ENST00000673771.1:c.78G>T	ENSP00000501023.1:p.Gly26=
ENST00000673774.1:n.774G>T
ENST00000673839.1:c.78G>T	ENSP00000501188.1:p.Gly26=
ENST00000673851.1:c.78G>T	ENSP00000501142.1:p.Gly26=
ENST00000673854.1:n.5495G>T
ENST00000673886.1:c.78G>T	ENSP00000501155.1:p.Gly26=
ENST00000673890.1:c.78G>T	ENSP00000501293.1:p.Gly26=
ENST00000673928.1:c.78G>T	ENSP00000501099.1:p.Gly26=
ENST00000673936.1:c.78G>T	ENSP00000501189.1:p.Gly26=
ENST00000673939.1:c.78G>T	ENSP00000501129.1:p.Gly26=
ENST00000673950.1:n.347G>T
ENST00000673978.1:c.216G>T	ENSP00000500976.1:p.Gly72=
ENST00000673987.1:c.78G>T	ENSP00000501231.1:p.Gly26=
ENST00000674011.1:c.78G>T	ENSP00000501171.1:p.Gly26=
ENST00000674018.1:c.78G>T	ENSP00000501271.1:p.Gly26=
ENST00000674027.1:n.133G>T
ENST00000674041.1:c.78G>T	ENSP00000500956.1:p.Gly26=
ENST00000674052.1:c.297G>T	ENSP00000501057.1:p.Gly99=
ENST00000674093.1:c.78G>T	ENSP00000501303.1:p.Gly26=
ENST00000674119.1:c.78G>T	ENSP00000501217.1:p.Gly26=
ENST00000674130.1:n.291G>T
ENST00000674135.1:c.255G>T	ENSP00000501178.1:p.Gly85=
ENST00000674139.1:c.78G>T	ENSP00000501054.1:p.Gly26=
ENST00000674146.1:c.78G>T	ENSP00000501175.1:p.Gly26=
ENST00000674149.1:c.78G>T	ENSP00000501112.1:p.Gly26=
ENST00000318023.11:c.1929G>T	ENSP00000326281.8:p.Gly643=
ENST00000337571.8:c.78G>T	ENSP00000336840.4:p.Gly26=
ENST00000349748.7:c.1797G>T	ENSP00000183936.4:p.Gly599=
ENST00000356316.7:c.78G>T	ENSP00000348667.4:p.Gly26=
ENST00000357568.7:c.2055G>T	ENSP00000350181.3:p.Gly685=
ENST00000397163.7:c.2073G>T	ENSP00000380349.3:p.Gly691=
ENST00000397200.8:c.537G>T	ENSP00000380384.4:p.Gly179=
ENST00000397204.8:c.78G>T	ENSP00000380387.4:p.Gly26=
ENST00000466222.6:n.996G>T
ENST00000561817.5:c.78G>T	ENSP00000456575.1:p.Gly26=
ENST00000562199.1:n.81G>T
ENST00000564503.5:c.170G>T
ENST00000565274.5:c.285G>T	ENSP00000457759.1:p.Gly95=
ENST00000565559.5:c.255G>T	ENSP00000457878.1:p.Gly85=
ENST00000567071.5:c.553G>T
ENST00000569136.5:c.78G>T	ENSP00000455254.1:p.Gly26=
ENST00000569827.5:c.405G>T	ENSP00000454379.1:p.Gly135=
NM_000070.2:c.2073G>T	NP_000061.1:p.Gly691=
NM_024344.1:c.2055G>T	NP_077320.1:p.Gly685=
NM_173087.1:c.1797G>T	NP_775110.1:p.Gly599=
NM_173088.1:c.537G>T	NP_775111.1:p.Gly179=
NM_173089.1:c.78G>T	NP_775112.1:p.Gly26=
NM_173090.1:c.78G>T	NP_775113.1:p.Gly26=
NM_000070.3:c.2073G>T MANE Select	NP_000061.1:p.Gly691=
NM_024344.2:c.2055G>T	NP_077320.1:p.Gly685=
NM_173087.2:c.1797G>T	NP_775110.1:p.Gly599=
NM_173088.2:c.537G>T	NP_775111.1:p.Gly179=
NM_173089.2:c.78G>T	NP_775112.1:p.Gly26=
NM_173090.2:c.78G>T	NP_775113.1:p.Gly26=