Canonical Allele Identifier: CA2645706422
Gene: CPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196757del , CM000663.2:g.53196757del GRCh38
NC_000001.10:g.53662429del , CM000663.1:g.53662429del GRCh37
NC_000001.9:g.53435017del NCBI36
NG_008035.1:g.5329del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-187del ENSP00000360541.3:n.-187del
NM_000098.2:c.-187del NP_000089.1:n.-187del
NM_001330589.1:c.-187del NP_001317518.1:n.-187del