Canonical Allele Identifier: CA2614740908

Gene: CPT1A

Linked Data

• gnomAD v4: 11-68759800-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68759800_68759801insA , CM000673.2:g.68759800_68759801insA	GRCh38
NC_000011.9:g.68527268_68527269insA , CM000673.1:g.68527268_68527269insA	GRCh37
NC_000011.8:g.68283844_68283845insA	NCBI36
NG_011801.1:g.87131_87132insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.2143-140_2143-139insT MANE Select	ENSP00000265641.4:n.2143-140_2143-139insT
ENST00000265641.9:c.2143-140_2143-139insT	ENSP00000265641.4:n.2143-140_2143-139insT
ENST00000376618.6:c.2143-140_2143-139insT	ENSP00000365803.2:n.2143-140_2143-139insT
ENST00000539743.5:c.2143-140_2143-139insT	ENSP00000446108.1:n.2143-140_2143-139insT
ENST00000540367.5:c.2143-140_2143-139insT	ENSP00000439084.1:n.2143-140_2143-139insT
NM_001031847.2:c.2143-140_2143-139insT	NP_001027017.1:n.2143-140_2143-139insT
NM_001876.3:c.2143-140_2143-139insT	NP_001867.2:n.2143-140_2143-139insT
XM_005273762.1:c.2239-140_2239-139insT	XP_005273819.1:n.2239-140_2239-139insT
XM_005273763.1:c.2239-140_2239-139insT	XP_005273820.1:n.2239-140_2239-139insT
XM_005273762.3:c.2239-140_2239-139insT	XP_005273819.1:n.2239-140_2239-139insT
XM_017017220.1:c.2143-140_2143-139insT	XP_016872709.1:n.2143-140_2143-139insT
NM_001876.4:c.2143-140_2143-139insT MANE Select	NP_001867.2:n.2143-140_2143-139insT
NM_001031847.3:c.2143-140_2143-139insT	NP_001027017.1:n.2143-140_2143-139insT