Canonical Allele Identifier: CA2792553347

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68793424_68793425dup , CM000673.2:g.68793424_68793425dup	GRCh38
NC_000011.9:g.68560892_68560893dup , CM000673.1:g.68560892_68560893dup	GRCh37
NC_000011.8:g.68317468_68317469dup	NCBI36
NG_011801.1:g.53508_53509dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.880-22_880-21dup MANE Select	ENSP00000265641.4:n.880-22_880-21dup
ENST00000265641.9:c.880-22_880-21dup	ENSP00000265641.4:n.880-22_880-21dup
ENST00000376618.6:c.880-22_880-21dup	ENSP00000365803.2:n.880-22_880-21dup
ENST00000538994.1:c.136-22_136-21dup	ENSP00000454332.1:n.136-22_136-21dup
ENST00000539743.5:c.880-22_880-21dup	ENSP00000446108.1:n.880-22_880-21dup
ENST00000540367.5:c.880-22_880-21dup	ENSP00000439084.1:n.880-22_880-21dup
NM_001031847.2:c.880-22_880-21dup	NP_001027017.1:n.880-22_880-21dup
NM_001876.3:c.880-22_880-21dup	NP_001867.2:n.880-22_880-21dup
XM_005273762.1:c.976-22_976-21dup	XP_005273819.1:n.976-22_976-21dup
XM_005273763.1:c.976-22_976-21dup	XP_005273820.1:n.976-22_976-21dup
XM_005273762.3:c.976-22_976-21dup	XP_005273819.1:n.976-22_976-21dup
XM_017017220.1:c.880-22_880-21dup	XP_016872709.1:n.880-22_880-21dup
NM_001876.4:c.880-22_880-21dup MANE Select	NP_001867.2:n.880-22_880-21dup
NM_001031847.3:c.880-22_880-21dup	NP_001027017.1:n.880-22_880-21dup