Canonical Allele Identifier: CA2792552362

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68759683_68759684insAAAAAAAATTTT , CM000673.2:g.68759683_68759684insAAAAAAAATTTT	GRCh38
NC_000011.9:g.68527151_68527152insAAAAAAAATTTT , CM000673.1:g.68527151_68527152insAAAAAAAATTTT	GRCh37
NC_000011.8:g.68283727_68283728insAAAAAAAATTTT	NCBI36
NG_011801.1:g.87248_87249insAAAATTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.2143-23_2143-22insAAAATTTTTTTT MANE Select	ENSP00000265641.4:n.2143-23_2143-22insAAAATTTTTTTT
ENST00000265641.9:c.2143-23_2143-22insAAAATTTTTTTT	ENSP00000265641.4:n.2143-23_2143-22insAAAATTTTTTTT
ENST00000376618.6:c.2143-23_2143-22insAAAATTTTTTTT	ENSP00000365803.2:n.2143-23_2143-22insAAAATTTTTTTT
ENST00000539743.5:c.2143-23_2143-22insAAAATTTTTTTT	ENSP00000446108.1:n.2143-23_2143-22insAAAATTTTTTTT
ENST00000540367.5:c.2143-23_2143-22insAAAATTTTTTTT	ENSP00000439084.1:n.2143-23_2143-22insAAAATTTTTTTT
NM_001031847.2:c.2143-23_2143-22insAAAATTTTTTTT	NP_001027017.1:n.2143-23_2143-22insAAAATTTTTTTT
NM_001876.3:c.2143-23_2143-22insAAAATTTTTTTT	NP_001867.2:n.2143-23_2143-22insAAAATTTTTTTT
XM_005273762.1:c.2239-23_2239-22insAAAATTTTTTTT	XP_005273819.1:n.2239-23_2239-22insAAAATTTTTTTT
XM_005273763.1:c.2239-23_2239-22insAAAATTTTTTTT	XP_005273820.1:n.2239-23_2239-22insAAAATTTTTTTT
XM_005273762.3:c.2239-23_2239-22insAAAATTTTTTTT	XP_005273819.1:n.2239-23_2239-22insAAAATTTTTTTT
XM_017017220.1:c.2143-23_2143-22insAAAATTTTTTTT	XP_016872709.1:n.2143-23_2143-22insAAAATTTTTTTT
NM_001876.4:c.2143-23_2143-22insAAAATTTTTTTT MANE Select	NP_001867.2:n.2143-23_2143-22insAAAATTTTTTTT
NM_001031847.3:c.2143-23_2143-22insAAAATTTTTTTT	NP_001027017.1:n.2143-23_2143-22insAAAATTTTTTTT