Canonical Allele Identifier: CA3182674357

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68815379A= , CM000673.2:g.68815379A=	GRCh38
NC_000011.9:g.68582847A= , CM000673.1:g.68582847A=	GRCh37
NC_000011.8:g.68339423A=	NCBI36
NG_011801.1:g.31553T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001876.4:c.96T= MANE Select	NP_001867.2:p.Tyr32=
ENST00000265641.10:c.96T= MANE Select	ENSP00000265641.4:p.Tyr32=
NM_001031847.2:c.96T=	NP_001027017.1:p.Tyr32=
NM_001031847.3:c.96T=	NP_001027017.1:p.Tyr32=
NM_001876.3:c.96T=	NP_001867.2:p.Tyr32=
ENST00000265641.9:c.96T=	ENSP00000265641.4:p.Tyr32=
ENST00000376618.6:c.96T=	ENSP00000365803.2:p.Tyr32=
ENST00000539743.5:c.96T=	ENSP00000446108.1:p.Tyr32=
ENST00000540367.5:c.96T=	ENSP00000439084.1:p.Tyr32=
ENST00000561996.1:c.96T=	ENSP00000457663.1:p.Tyr32=
ENST00000565318.5:c.96T=	ENSP00000457826.1:p.Tyr32=
ENST00000569129.5:c.96T=	ENSP00000455116.1:p.Tyr32=
XM_005273762.1:c.192T=	XP_005273819.1:p.Tyr64=
XM_005273762.3:c.192T=	XP_005273819.1:p.Tyr64=
XM_005273763.1:c.192T=	XP_005273820.1:p.Tyr64=
XM_017017220.1:c.96T=	XP_016872709.1:p.Tyr32=