Canonical Allele Identifier: CA1167208735
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs1645321139

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196660dup , CM000663.2:g.53196660dup GRCh38
NC_000001.10:g.53662332dup , CM000663.1:g.53662332dup GRCh37
NC_000001.9:g.53434920dup NCBI36
NG_008035.1:g.5232dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-284dup ENSP00000360541.3:n.-284dup
NM_000098.2:c.-284dup NP_000089.1:n.-284dup
NM_001330589.1:c.-284dup NP_001317518.1:n.-284dup