Canonical Allele Identifier: CA3182674349

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68804077G= , CM000673.2:g.68804077G=	GRCh38
NC_000011.9:g.68571545G= , CM000673.1:g.68571545G=	GRCh37
NC_000011.8:g.68328121G=	NCBI36
NG_011801.1:g.42855C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.478C= MANE Select	ENSP00000265641.4:p.Arg160=
ENST00000265641.9:c.478C=	ENSP00000265641.4:p.Arg160=
ENST00000376618.6:c.478C=	ENSP00000365803.2:p.Arg160=
ENST00000539743.5:c.478C=	ENSP00000446108.1:p.Arg160=
ENST00000540367.5:c.478C=	ENSP00000439084.1:p.Arg160=
NM_001031847.2:c.478C=	NP_001027017.1:p.Arg160=
NM_001876.3:c.478C=	NP_001867.2:p.Arg160=
XM_005273762.1:c.574C=	XP_005273819.1:p.Arg192=
XM_005273763.1:c.574C=	XP_005273820.1:p.Arg192=
XM_005273762.3:c.574C=	XP_005273819.1:p.Arg192=
XM_017017220.1:c.478C=	XP_016872709.1:p.Arg160=
NM_001876.4:c.478C= MANE Select	NP_001867.2:p.Arg160=
NM_001031847.3:c.478C=	NP_001027017.1:p.Arg160=