Canonical Allele Identifier: CA1167208701

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53196586_53196588delinsCTT , CM000663.2:g.53196586_53196588delinsCTT	GRCh38
NC_000001.10:g.53662258_53662260delinsCTT , CM000663.1:g.53662258_53662260delinsCTT	GRCh37
NC_000001.9:g.53434846_53434848delinsCTT	NCBI36
NG_008035.1:g.5158_5160delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.3:c.-358_-356delinsCTT	ENSP00000360541.3:n.-358_-356delinsCTT
NM_000098.2:c.-358_-356delinsCTT	NP_000089.1:n.-358_-356delinsCTT
NM_001330589.1:c.-358_-356delinsCTT	NP_001317518.1:n.-358_-356delinsCTT