Canonical Allele Identifier: CA1167208746
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs1645321314

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196676_53196679del , CM000663.2:g.53196676_53196679del GRCh38
NC_000001.10:g.53662348_53662351del , CM000663.1:g.53662348_53662351del GRCh37
NC_000001.9:g.53434936_53434939del NCBI36
NG_008035.1:g.5248_5251del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-268_-265del ENSP00000360541.3:n.-268_-265del
NM_000098.2:c.-268_-265del NP_000089.1:n.-268_-265del
NM_001330589.1:c.-268_-265del NP_001317518.1:n.-268_-265del