Canonical Allele Identifier: CA1167208774

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53196704_53196705delinsGC , CM000663.2:g.53196704_53196705delinsGC	GRCh38
NC_000001.10:g.53662376_53662377delinsGC , CM000663.1:g.53662376_53662377delinsGC	GRCh37
NC_000001.9:g.53434964_53434965delinsGC	NCBI36
NG_008035.1:g.5276_5277delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.3:c.-240_-239delinsGC	ENSP00000360541.3:n.-240_-239delinsGC
NM_000098.2:c.-240_-239delinsGC	NP_000089.1:n.-240_-239delinsGC
NM_001330589.1:c.-240_-239delinsGC	NP_001317518.1:n.-240_-239delinsGC