Canonical Allele Identifier: CA1148415070

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53196587_53196596delinsTTTTTTTTTT , CM000663.2:g.53196587_53196596delinsTTTTTTTTTT	GRCh38
NC_000001.10:g.53662259_53662268delinsTTTTTTTTTT , CM000663.1:g.53662259_53662268delinsTTTTTTTTTT	GRCh37
NC_000001.9:g.53434847_53434856delinsTTTTTTTTTT	NCBI36
NG_008035.1:g.5159_5168delinsTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.3:c.-357_-348delinsTTTTTTTTTT	ENSP00000360541.3:n.-357_-348delinsTTTTTTTTTT
NM_000098.2:c.-357_-348delinsTTTTTTTTTT	NP_000089.1:n.-357_-348delinsTTTTTTTTTT
NM_001330589.1:c.-357_-348delinsTTTTTTTTTT	NP_001317518.1:n.-357_-348delinsTTTTTTTTTT