Canonical Allele Identifier: CA2645706311
Gene: CPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196627_53196628del , CM000663.2:g.53196627_53196628del GRCh38
NC_000001.10:g.53662299_53662300del , CM000663.1:g.53662299_53662300del GRCh37
NC_000001.9:g.53434887_53434888del NCBI36
NG_008035.1:g.5199_5200del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-317_-316del ENSP00000360541.3:n.-317_-316del
NM_000098.2:c.-317_-316del NP_000089.1:n.-317_-316del
NM_001330589.1:c.-317_-316del NP_001317518.1:n.-317_-316del