Canonical Allele Identifier: CA1167208722
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196637_53196638delinsGC , CM000663.2:g.53196637_53196638delinsGC GRCh38
NC_000001.10:g.53662309_53662310delinsGC , CM000663.1:g.53662309_53662310delinsGC GRCh37
NC_000001.9:g.53434897_53434898delinsGC NCBI36
NG_008035.1:g.5209_5210delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-307_-306delinsGC ENSP00000360541.3:n.-307_-306delinsGC
NM_000098.2:c.-307_-306delinsGC NP_000089.1:n.-307_-306delinsGC
NM_001330589.1:c.-307_-306delinsGC NP_001317518.1:n.-307_-306delinsGC