Canonical Allele Identifier: CA2697552429

Gene: CPT2

Linked Data

• ClinVar Variation Id: 2693653
• ClinVar RCV Id: RCV003581961

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210637del , CM000663.2:g.53210637del	GRCh38
NC_000001.10:g.53676309del , CM000663.1:g.53676309del	GRCh37
NC_000001.9:g.53448897del	NCBI36
NG_008035.1:g.19209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.963del MANE Select	ENSP00000360541.3:p.Val322CysfsTer6
ENST00000635862.1:c.963del	ENSP00000490867.1:p.Val322CysfsTer6
ENST00000635888.1:c.*949del	ENSP00000490042.1:n.*949del
ENST00000636239.1:c.*610del	ENSP00000490066.1:n.*610del
ENST00000636867.1:c.963del	ENSP00000489631.1:p.Val322CysfsTer6
ENST00000636891.1:c.963del	ENSP00000490399.1:p.Val322CysfsTer6
ENST00000636935.1:c.341-2627del	ENSP00000489757.1:n.341-2627del
ENST00000637252.1:c.963del	ENSP00000490492.1:p.Val322CysfsTer6
ENST00000637726.1:n.3163del
ENST00000638135.1:c.*610del	ENSP00000489756.1:n.*610del
ENST00000371486.3:c.963del	ENSP00000360541.3:p.Val322CysfsTer6
NM_000098.2:c.963del	NP_000089.1:p.Val322CysfsTer6
XM_005270484.1:c.963del	XP_005270541.1:p.Val322CysfsTer6
NM_001330589.1:c.963del	NP_001317518.1:p.Val322CysfsTer6
NM_000098.3:c.963del MANE Select	NP_000089.1:p.Val322CysfsTer6
NM_001330589.2:c.963del	NP_001317518.1:p.Val322CysfsTer6