Canonical Allele Identifier: CA2645706276
Gene: CPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196595_53196596insC , CM000663.2:g.53196595_53196596insC GRCh38
NC_000001.10:g.53662267_53662268insC , CM000663.1:g.53662267_53662268insC GRCh37
NC_000001.9:g.53434855_53434856insC NCBI36
NG_008035.1:g.5167_5168insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-349_-348insC ENSP00000360541.3:n.-349_-348insC
NM_000098.2:c.-349_-348insC NP_000089.1:n.-349_-348insC
NM_001330589.1:c.-349_-348insC NP_001317518.1:n.-349_-348insC