Canonical Allele Identifier: CA2839661218

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68760195dup , CM000673.2:g.68760195dup	GRCh38
NC_000011.9:g.68527663dup , CM000673.1:g.68527663dup	GRCh37
NC_000011.8:g.68284239dup	NCBI36
NG_011801.1:g.86737dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.2142+30dup MANE Select	ENSP00000265641.4:n.2142+30dup
ENST00000265641.9:c.2142+30dup	ENSP00000265641.4:n.2142+30dup
ENST00000376618.6:c.2142+30dup	ENSP00000365803.2:n.2142+30dup
ENST00000539743.5:c.2142+30dup	ENSP00000446108.1:n.2142+30dup
ENST00000540367.5:c.2142+30dup	ENSP00000439084.1:n.2142+30dup
NM_001031847.2:c.2142+30dup	NP_001027017.1:n.2142+30dup
NM_001876.3:c.2142+30dup	NP_001867.2:n.2142+30dup
XM_005273762.1:c.2238+30dup	XP_005273819.1:n.2238+30dup
XM_005273763.1:c.2238+30dup	XP_005273820.1:n.2238+30dup
XM_005273762.3:c.2238+30dup	XP_005273819.1:n.2238+30dup
XM_017017220.1:c.2142+30dup	XP_016872709.1:n.2142+30dup
NM_001876.4:c.2142+30dup MANE Select	NP_001867.2:n.2142+30dup
NM_001031847.3:c.2142+30dup	NP_001027017.1:n.2142+30dup