Canonical Allele Identifier: CA1167208869

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53196823_53196826delinsCGGA , CM000663.2:g.53196823_53196826delinsCGGA	GRCh38
NC_000001.10:g.53662495_53662498delinsCGGA , CM000663.1:g.53662495_53662498delinsCGGA	GRCh37
NC_000001.9:g.53435083_53435086delinsCGGA	NCBI36
NG_008035.1:g.5395_5398delinsCGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635862.1:c.-121_-118delinsCGGA	ENSP00000490867.1:n.-121_-118delinsCGGA
ENST00000635888.1:c.-121_-118delinsCGGA	ENSP00000490042.1:n.-121_-118delinsCGGA
ENST00000636239.1:c.-121_-118delinsCGGA	ENSP00000490066.1:n.-121_-118delinsCGGA
ENST00000636867.1:c.-121_-118delinsCGGA	ENSP00000489631.1:n.-121_-118delinsCGGA
ENST00000636891.1:c.-121_-118delinsCGGA	ENSP00000490399.1:n.-121_-118delinsCGGA
ENST00000636935.1:c.-121_-118delinsCGGA	ENSP00000489757.1:n.-121_-118delinsCGGA
ENST00000637252.1:c.-121_-118delinsCGGA	ENSP00000490492.1:n.-121_-118delinsCGGA
ENST00000371486.3:c.-121_-118delinsCGGA	ENSP00000360541.3:n.-121_-118delinsCGGA
NM_000098.2:c.-121_-118delinsCGGA	NP_000089.1:n.-121_-118delinsCGGA
XM_005270484.1:c.-121_-118delinsCGGA	XP_005270541.1:n.-121_-118delinsCGGA
NM_001330589.1:c.-121_-118delinsCGGA	NP_001317518.1:n.-121_-118delinsCGGA