Canonical Allele Identifier: CA2792553641

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68804133del , CM000673.2:g.68804133del	GRCh38
NC_000011.9:g.68571601del , CM000673.1:g.68571601del	GRCh37
NC_000011.8:g.68328177del	NCBI36
NG_011801.1:g.42799del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.454-32del MANE Select	ENSP00000265641.4:n.454-32del
ENST00000265641.9:c.454-32del	ENSP00000265641.4:n.454-32del
ENST00000376618.6:c.454-32del	ENSP00000365803.2:n.454-32del
ENST00000539743.5:c.454-32del	ENSP00000446108.1:n.454-32del
ENST00000540367.5:c.454-32del	ENSP00000439084.1:n.454-32del
NM_001031847.2:c.454-32del	NP_001027017.1:n.454-32del
NM_001876.3:c.454-32del	NP_001867.2:n.454-32del
XM_005273762.1:c.550-32del	XP_005273819.1:n.550-32del
XM_005273763.1:c.550-32del	XP_005273820.1:n.550-32del
XM_005273762.3:c.550-32del	XP_005273819.1:n.550-32del
XM_017017220.1:c.454-32del	XP_016872709.1:n.454-32del
NM_001876.4:c.454-32del MANE Select	NP_001867.2:n.454-32del
NM_001031847.3:c.454-32del	NP_001027017.1:n.454-32del