Canonical Allele Identifier: CA2976665830

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68794793dup , CM000673.2:g.68794793dup	GRCh38
NC_000011.9:g.68562261dup , CM000673.1:g.68562261dup	GRCh37
NC_000011.8:g.68318837dup	NCBI36
NG_011801.1:g.52141dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.879+13dup MANE Select	ENSP00000265641.4:n.879+13dup
ENST00000265641.9:c.879+13dup	ENSP00000265641.4:n.879+13dup
ENST00000376618.6:c.879+13dup	ENSP00000365803.2:n.879+13dup
ENST00000538994.1:c.135+13dup	ENSP00000454332.1:n.135+13dup
ENST00000539743.5:c.879+13dup	ENSP00000446108.1:n.879+13dup
ENST00000540367.5:c.879+13dup	ENSP00000439084.1:n.879+13dup
NM_001031847.2:c.879+13dup	NP_001027017.1:n.879+13dup
NM_001876.3:c.879+13dup	NP_001867.2:n.879+13dup
XM_005273762.1:c.975+13dup	XP_005273819.1:n.975+13dup
XM_005273763.1:c.975+13dup	XP_005273820.1:n.975+13dup
XM_005273762.3:c.975+13dup	XP_005273819.1:n.975+13dup
XM_017017220.1:c.879+13dup	XP_016872709.1:n.879+13dup
NM_001876.4:c.879+13dup MANE Select	NP_001867.2:n.879+13dup
NM_001031847.3:c.879+13dup	NP_001027017.1:n.879+13dup