Canonical Allele Identifier: CA1167215341

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210894_53210896delinsACT , CM000663.2:g.53210894_53210896delinsACT	GRCh38
NC_000001.10:g.53676566_53676568delinsACT , CM000663.1:g.53676566_53676568delinsACT	GRCh37
NC_000001.9:g.53449154_53449156delinsACT	NCBI36
NG_008035.1:g.19466_19468delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1220_1222delinsACT MANE Select	ENSP00000360541.3:p.Asp407=
ENST00000635862.1:c.1220_1222delinsACT	ENSP00000490867.1:p.Asp407=
ENST00000635888.1:c.*1206_*1208delinsACT	ENSP00000490042.1:n.*1206_*1208delinsACT
ENST00000636239.1:c.*867_*869delinsACT	ENSP00000490066.1:n.*867_*869delinsACT
ENST00000636867.1:c.1220_1222delinsACT	ENSP00000489631.1:p.Asp407=
ENST00000636891.1:c.1220_1222delinsACT	ENSP00000490399.1:p.Asp407=
ENST00000636935.1:c.341-2370_341-2368delinsACT	ENSP00000489757.1:n.341-2370_341-2368delinsACT
ENST00000637252.1:c.1220_1222delinsACT	ENSP00000490492.1:p.Asp407=
ENST00000637726.1:n.3420_3422delinsACT
ENST00000638135.1:c.*867_*869delinsACT	ENSP00000489756.1:n.*867_*869delinsACT
ENST00000371486.3:c.1220_1222delinsACT	ENSP00000360541.3:p.Asp407=
NM_000098.2:c.1220_1222delinsACT	NP_000089.1:p.Asp407=
XM_005270484.1:c.1220_1222delinsACT	XP_005270541.1:p.Asp407=
NM_001330589.1:c.1220_1222delinsACT	NP_001317518.1:p.Asp407=
NM_000098.3:c.1220_1222delinsACT MANE Select	NP_000089.1:p.Asp407=
NM_001330589.2:c.1220_1222delinsACT	NP_001317518.1:p.Asp407=