Canonical Allele Identifier: CA1167208755
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196685_53196686delinsGA , CM000663.2:g.53196685_53196686delinsGA GRCh38
NC_000001.10:g.53662357_53662358delinsGA , CM000663.1:g.53662357_53662358delinsGA GRCh37
NC_000001.9:g.53434945_53434946delinsGA NCBI36
NG_008035.1:g.5257_5258delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-259_-258delinsGA ENSP00000360541.3:n.-259_-258delinsGA
NM_000098.2:c.-259_-258delinsGA NP_000089.1:n.-259_-258delinsGA
NM_001330589.1:c.-259_-258delinsGA NP_001317518.1:n.-259_-258delinsGA