Canonical Allele Identifier: CA6093141
Gene: CAPN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65186194G>A , CM000673.2:g.65186194G>A GRCh38
NC_000011.9:g.64953665G>A , CM000673.1:g.64953665G>A GRCh37
NC_000011.8:g.64710241G>A NCBI36
NG_052817.1:g.9980G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000279247.11:c.615G>A MANE Select ENSP00000279247.7:p.Leu205=
ENST00000279247.10:c.615G>A ENSP00000279247.6:p.Leu205=
ENST00000524773.5:c.615G>A ENSP00000434176.1:p.Leu205=
ENST00000526468.1:c.300G>A ENSP00000433366.1:p.Leu100=
ENST00000526954.5:c.590+144G>A ENSP00000436002.1:n.590+144G>A
ENST00000527323.5:c.615G>A ENSP00000431984.1:p.Leu205=
ENST00000527897.1:n.263G>A
ENST00000533129.5:c.615G>A ENSP00000431686.1:p.Leu205=
ENST00000533820.5:c.615G>A ENSP00000435272.1:p.Leu205=
NM_001198868.1:c.615G>A NP_001185797.1:p.Leu205=
NM_001198869.1:c.615G>A NP_001185798.1:p.Leu205=
NM_005186.3:c.615G>A NP_005177.2:p.Leu205=
NR_040008.1:n.727G>A
XM_006718698.1:c.615G>A XP_006718761.1:p.Leu205=
XM_011545292.1:c.615G>A XP_011543594.1:p.Leu205=
XM_006718698.2:c.615G>A XP_006718761.1:p.Leu205=
NM_001198868.2:c.615G>A NP_001185797.1:p.Leu205=
NM_005186.4:c.615G>A MANE Select NP_005177.2:p.Leu205=
NR_040008.2:n.632G>A
NM_001198869.2:c.615G>A NP_001185798.1:p.Leu205=