Canonical Allele Identifier: CA2645706277
Gene: CPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196597_53196601del , CM000663.2:g.53196597_53196601del GRCh38
NC_000001.10:g.53662269_53662273del , CM000663.1:g.53662269_53662273del GRCh37
NC_000001.9:g.53434857_53434861del NCBI36
NG_008035.1:g.5169_5173del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-347_-343del ENSP00000360541.3:n.-347_-343del
NM_000098.2:c.-347_-343del NP_000089.1:n.-347_-343del
NM_001330589.1:c.-347_-343del NP_001317518.1:n.-347_-343del