Canonical Allele Identifier: CA2645711442
Gene: CPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53210110_53210112del , CM000663.2:g.53210110_53210112del GRCh38
NC_000001.10:g.53675782_53675784del , CM000663.1:g.53675782_53675784del GRCh37
NC_000001.9:g.53448370_53448372del NCBI36
NG_008035.1:g.18682_18684del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.4:c.436_438del MANE Select ENSP00000360541.3:p.Asn146del
ENST00000635862.1:c.436_438del ENSP00000490867.1:p.Asn146del
ENST00000635888.1:c.*422_*424del ENSP00000490042.1:n.*422_*424del
ENST00000636239.1:c.*83_*85del ENSP00000490066.1:n.*83_*85del
ENST00000636867.1:c.436_438del ENSP00000489631.1:p.Asn146del
ENST00000636891.1:c.436_438del ENSP00000490399.1:p.Asn146del
ENST00000636935.1:c.341-3154_341-3152del ENSP00000489757.1:n.341-3154_341-3152del
ENST00000637252.1:c.436_438del ENSP00000490492.1:p.Asn146del
ENST00000637726.1:n.2636_2638del
ENST00000638135.1:c.*83_*85del ENSP00000489756.1:n.*83_*85del
ENST00000371486.3:c.436_438del ENSP00000360541.3:p.Asn146del
NM_000098.2:c.436_438del NP_000089.1:p.Asn146del
XM_005270484.1:c.436_438del XP_005270541.1:p.Asn146del
NM_001330589.1:c.436_438del NP_001317518.1:p.Asn146del
NM_000098.3:c.436_438del MANE Select NP_000089.1:p.Asn146del
NM_001330589.2:c.436_438del NP_001317518.1:p.Asn146del