Canonical Allele Identifier: CA2645706347
Gene: CPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196677_53196681dup , CM000663.2:g.53196677_53196681dup GRCh38
NC_000001.10:g.53662349_53662353dup , CM000663.1:g.53662349_53662353dup GRCh37
NC_000001.9:g.53434937_53434941dup NCBI36
NG_008035.1:g.5249_5253dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-267_-263dup ENSP00000360541.3:n.-267_-263dup
NM_000098.2:c.-267_-263dup NP_000089.1:n.-267_-263dup
NM_001330589.1:c.-267_-263dup NP_001317518.1:n.-267_-263dup