Canonical Allele Identifier: CA2507351766

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53209983_53209984insAAAATG , CM000663.2:g.53209983_53209984insAAAATG	GRCh38
NC_000001.10:g.53675655_53675656insAAAATG , CM000663.1:g.53675655_53675656insAAAATG	GRCh37
NC_000001.9:g.53448243_53448244insAAAATG	NCBI36
NG_008035.1:g.18555_18556insAAAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.341-32_341-31insAAAATG MANE Select	ENSP00000360541.3:n.341-32_341-31insAAAATG
ENST00000635862.1:c.341-32_341-31insAAAATG	ENSP00000490867.1:n.341-32_341-31insAAAATG
ENST00000635888.1:c.*327-32_*327-31insAAAATG	ENSP00000490042.1:n.*327-32_*327-31insAAAATG
ENST00000636239.1:c.234-32_234-31insAAAATG	ENSP00000490066.1:n.234-32_234-31insAAAATG
ENST00000636867.1:c.341-32_341-31insAAAATG	ENSP00000489631.1:n.341-32_341-31insAAAATG
ENST00000636891.1:c.341-32_341-31insAAAATG	ENSP00000490399.1:n.341-32_341-31insAAAATG
ENST00000636935.1:c.341-3281_341-3280insAAAATG	ENSP00000489757.1:n.341-3281_341-3280insAAAATG
ENST00000637252.1:c.341-32_341-31insAAAATG	ENSP00000490492.1:n.341-32_341-31insAAAATG
ENST00000637726.1:n.2509_2510insAAAATG
ENST00000638135.1:c.153-32_153-31insAAAATG	ENSP00000489756.1:n.153-32_153-31insAAAATG
ENST00000371486.3:c.341-32_341-31insAAAATG	ENSP00000360541.3:n.341-32_341-31insAAAATG
NM_000098.2:c.341-32_341-31insAAAATG	NP_000089.1:n.341-32_341-31insAAAATG
XM_005270484.1:c.341-32_341-31insAAAATG	XP_005270541.1:n.341-32_341-31insAAAATG
NM_001330589.1:c.341-32_341-31insAAAATG	NP_001317518.1:n.341-32_341-31insAAAATG
NM_000098.3:c.341-32_341-31insAAAATG MANE Select	NP_000089.1:n.341-32_341-31insAAAATG
NM_001330589.2:c.341-32_341-31insAAAATG	NP_001317518.1:n.341-32_341-31insAAAATG