Canonical Allele Identifier: CA3182864118

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68796900G= , CM000673.2:g.68796900G=	GRCh38
NC_000011.9:g.68564368G= , CM000673.1:g.68564368G=	GRCh37
NC_000011.8:g.68320944G=	NCBI36
NG_011801.1:g.50032C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001876.4:c.727C= MANE Select	NP_001867.2:p.Arg243=
ENST00000265641.10:c.727C= MANE Select	ENSP00000265641.4:p.Arg243=
NM_001031847.2:c.727C=	NP_001027017.1:p.Arg243=
NM_001031847.3:c.727C=	NP_001027017.1:p.Arg243=
NM_001876.3:c.727C=	NP_001867.2:p.Arg243=
ENST00000265641.9:c.727C=	ENSP00000265641.4:p.Arg243=
ENST00000376618.6:c.727C=	ENSP00000365803.2:p.Arg243=
ENST00000538994.1:c.-18C=	ENSP00000454332.1:n.-18C=
ENST00000539743.5:c.727C=	ENSP00000446108.1:p.Arg243=
ENST00000540367.5:c.727C=	ENSP00000439084.1:p.Arg243=
XM_005273762.1:c.823C=	XP_005273819.1:p.Arg275=
XM_005273762.3:c.823C=	XP_005273819.1:p.Arg275=
XM_005273763.1:c.823C=	XP_005273820.1:p.Arg275=
XM_017017220.1:c.727C=	XP_016872709.1:p.Arg243=