Canonical Allele Identifier: CA2645706285
Gene: CPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196604_53196605del , CM000663.2:g.53196604_53196605del GRCh38
NC_000001.10:g.53662276_53662277del , CM000663.1:g.53662276_53662277del GRCh37
NC_000001.9:g.53434864_53434865del NCBI36
NG_008035.1:g.5176_5177del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-340_-339del ENSP00000360541.3:n.-340_-339del
NM_000098.2:c.-340_-339del NP_000089.1:n.-340_-339del
NM_001330589.1:c.-340_-339del NP_001317518.1:n.-340_-339del