Canonical Allele Identifier: CA1001798169
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs1645321441

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196686del , CM000663.2:g.53196686del GRCh38
NC_000001.10:g.53662358del , CM000663.1:g.53662358del GRCh37
NC_000001.9:g.53434946del NCBI36
NG_008035.1:g.5258del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-258del ENSP00000360541.3:n.-258del
NM_000098.2:c.-258del NP_000089.1:n.-258del
NM_001330589.1:c.-258del NP_001317518.1:n.-258del