Canonical Allele Identifier: CA2614737469
Gene: CPT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68793501_68793502insG , CM000673.2:g.68793501_68793502insG GRCh38
NC_000011.9:g.68560969_68560970insG , CM000673.1:g.68560969_68560970insG GRCh37
NC_000011.8:g.68317545_68317546insG NCBI36
NG_011801.1:g.53430_53431insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265641.10:c.880-100_880-99insC MANE Select ENSP00000265641.4:n.880-100_880-99insC
ENST00000265641.9:c.880-100_880-99insC ENSP00000265641.4:n.880-100_880-99insC
ENST00000376618.6:c.880-100_880-99insC ENSP00000365803.2:n.880-100_880-99insC
ENST00000538994.1:c.136-100_136-99insC ENSP00000454332.1:n.136-100_136-99insC
ENST00000539743.5:c.880-100_880-99insC ENSP00000446108.1:n.880-100_880-99insC
ENST00000540367.5:c.880-100_880-99insC ENSP00000439084.1:n.880-100_880-99insC
NM_001031847.2:c.880-100_880-99insC NP_001027017.1:n.880-100_880-99insC
NM_001876.3:c.880-100_880-99insC NP_001867.2:n.880-100_880-99insC
XM_005273762.1:c.976-100_976-99insC XP_005273819.1:n.976-100_976-99insC
XM_005273763.1:c.976-100_976-99insC XP_005273820.1:n.976-100_976-99insC
XM_005273762.3:c.976-100_976-99insC XP_005273819.1:n.976-100_976-99insC
XM_017017220.1:c.880-100_880-99insC XP_016872709.1:n.880-100_880-99insC
NM_001876.4:c.880-100_880-99insC MANE Select NP_001867.2:n.880-100_880-99insC
NM_001031847.3:c.880-100_880-99insC NP_001027017.1:n.880-100_880-99insC