Canonical Allele Identifier: CA3183114568

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68807639C= , CM000673.2:g.68807639C=	GRCh38
NC_000011.9:g.68575107C= , CM000673.1:g.68575107C=	GRCh37
NC_000011.8:g.68331683C=	NCBI36
NG_011801.1:g.39293G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001876.4:c.282-1G= MANE Select	NP_001867.2:n.282-1G=
ENST00000265641.10:c.282-1G= MANE Select	ENSP00000265641.4:n.282-1G=
NM_001031847.2:c.282-1G=	NP_001027017.1:n.282-1G=
NM_001031847.3:c.282-1G=	NP_001027017.1:n.282-1G=
NM_001876.3:c.282-1G=	NP_001867.2:n.282-1G=
ENST00000265641.9:c.282-1G=	ENSP00000265641.4:n.282-1G=
ENST00000376618.6:c.282-1G=	ENSP00000365803.2:n.282-1G=
ENST00000539743.5:c.282-1G=	ENSP00000446108.1:n.282-1G=
ENST00000540367.5:c.282-1G=	ENSP00000439084.1:n.282-1G=
ENST00000565318.5:c.282-1G=	ENSP00000457826.1:n.282-1G=
ENST00000569129.5:c.282-1G=	ENSP00000455116.1:n.282-1G=
XM_005273762.1:c.378-1G=	XP_005273819.1:n.378-1G=
XM_005273762.3:c.378-1G=	XP_005273819.1:n.378-1G=
XM_005273763.1:c.378-1G=	XP_005273820.1:n.378-1G=
XM_017017220.1:c.282-1G=	XP_016872709.1:n.282-1G=