Canonical Allele Identifier: CA2581028861

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68789314G= , CM000673.2:g.68789314G=	GRCh38
NC_000011.9:g.68556782G= , CM000673.1:g.68556782G=	GRCh37
NC_000011.8:g.68313358G=	NCBI36
NG_011801.1:g.57618C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001876.4:c.967+4001C= MANE Select	NP_001867.2:n.967+4001C=
ENST00000265641.10:c.967+4001C= MANE Select	ENSP00000265641.4:n.967+4001C=
NM_001031847.2:c.967+4001C=	NP_001027017.1:n.967+4001C=
NM_001031847.3:c.967+4001C=	NP_001027017.1:n.967+4001C=
NM_001876.3:c.967+4001C=	NP_001867.2:n.967+4001C=
ENST00000265641.9:c.967+4001C=	ENSP00000265641.4:n.967+4001C=
ENST00000376618.6:c.967+4001C=	ENSP00000365803.2:n.967+4001C=
ENST00000538994.1:c.224-3279C=	ENSP00000454332.1:n.224-3279C=
ENST00000539743.5:c.967+4001C=	ENSP00000446108.1:n.967+4001C=
ENST00000540367.5:c.967+4001C=	ENSP00000439084.1:n.967+4001C=
XM_005273762.1:c.1063+4001C=	XP_005273819.1:n.1063+4001C=
XM_005273762.3:c.1063+4001C=	XP_005273819.1:n.1063+4001C=
XM_005273763.1:c.1063+4001C=	XP_005273820.1:n.1063+4001C=
XM_017017220.1:c.967+4001C=	XP_016872709.1:n.967+4001C=