Canonical Allele Identifier: CA2792553354

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68793528_68793529insTTTG , CM000673.2:g.68793528_68793529insTTTG	GRCh38
NC_000011.9:g.68560996_68560997insTTTG , CM000673.1:g.68560996_68560997insTTTG	GRCh37
NC_000011.8:g.68317572_68317573insTTTG	NCBI36
NG_011801.1:g.53404_53405insAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.880-126_880-125insAAAC MANE Select	ENSP00000265641.4:n.880-126_880-125insAAAC
ENST00000265641.9:c.880-126_880-125insAAAC	ENSP00000265641.4:n.880-126_880-125insAAAC
ENST00000376618.6:c.880-126_880-125insAAAC	ENSP00000365803.2:n.880-126_880-125insAAAC
ENST00000538994.1:c.136-126_136-125insAAAC	ENSP00000454332.1:n.136-126_136-125insAAAC
ENST00000539743.5:c.880-126_880-125insAAAC	ENSP00000446108.1:n.880-126_880-125insAAAC
ENST00000540367.5:c.880-126_880-125insAAAC	ENSP00000439084.1:n.880-126_880-125insAAAC
NM_001031847.2:c.880-126_880-125insAAAC	NP_001027017.1:n.880-126_880-125insAAAC
NM_001876.3:c.880-126_880-125insAAAC	NP_001867.2:n.880-126_880-125insAAAC
XM_005273762.1:c.976-126_976-125insAAAC	XP_005273819.1:n.976-126_976-125insAAAC
XM_005273763.1:c.976-126_976-125insAAAC	XP_005273820.1:n.976-126_976-125insAAAC
XM_005273762.3:c.976-126_976-125insAAAC	XP_005273819.1:n.976-126_976-125insAAAC
XM_017017220.1:c.880-126_880-125insAAAC	XP_016872709.1:n.880-126_880-125insAAAC
NM_001876.4:c.880-126_880-125insAAAC MANE Select	NP_001867.2:n.880-126_880-125insAAAC
NM_001031847.3:c.880-126_880-125insAAAC	NP_001027017.1:n.880-126_880-125insAAAC