Canonical Allele Identifier: CA3183114540

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68773294G= , CM000673.2:g.68773294G=	GRCh38
NC_000011.9:g.68540762G= , CM000673.1:g.68540762G=	GRCh37
NC_000011.8:g.68297338G=	NCBI36
NG_011801.1:g.73638C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001876.4:c.1711C= MANE Select	NP_001867.2:p.Gln571=
ENST00000265641.10:c.1711C= MANE Select	ENSP00000265641.4:p.Gln571=
NM_001031847.2:c.1711C=	NP_001027017.1:p.Gln571=
NM_001031847.3:c.1711C=	NP_001027017.1:p.Gln571=
NM_001876.3:c.1711C=	NP_001867.2:p.Gln571=
ENST00000265641.9:c.1711C=	ENSP00000265641.4:p.Gln571=
ENST00000376618.6:c.1711C=	ENSP00000365803.2:p.Gln571=
ENST00000537756.2:n.421C=
ENST00000539743.5:c.1711C=	ENSP00000446108.1:p.Gln571=
ENST00000540367.5:c.1711C=	ENSP00000439084.1:p.Gln571=
XM_005273762.1:c.1807C=	XP_005273819.1:p.Gln603=
XM_005273762.3:c.1807C=	XP_005273819.1:p.Gln603=
XM_005273763.1:c.1807C=	XP_005273820.1:p.Gln603=
XM_017017220.1:c.1711C=	XP_016872709.1:p.Gln571=