Canonical Allele Identifier: CA2645706306
Gene: CPT2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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