Canonical Allele Identifier: CA2574903061

Gene: CPT1A

Linked Data

• gnomAD v4: 11-68760145-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68760145A>T , CM000673.2:g.68760145A>T	GRCh38
NC_000011.9:g.68527613A>T , CM000673.1:g.68527613A>T	GRCh37
NC_000011.8:g.68284189A>T	NCBI36
NG_011801.1:g.86787T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265641.10:c.2142+80T>A MANE Select	ENSP00000265641.4:n.2142+80T>A
ENST00000265641.9:c.2142+80T>A	ENSP00000265641.4:n.2142+80T>A
ENST00000376618.6:c.2142+80T>A	ENSP00000365803.2:n.2142+80T>A
ENST00000539743.5:c.2142+80T>A	ENSP00000446108.1:n.2142+80T>A
ENST00000540367.5:c.2142+80T>A	ENSP00000439084.1:n.2142+80T>A
NM_001031847.2:c.2142+80T>A	NP_001027017.1:n.2142+80T>A
NM_001876.3:c.2142+80T>A	NP_001867.2:n.2142+80T>A
XM_005273762.1:c.2238+80T>A	XP_005273819.1:n.2238+80T>A
XM_005273763.1:c.2238+80T>A	XP_005273820.1:n.2238+80T>A
XM_005273762.3:c.2238+80T>A	XP_005273819.1:n.2238+80T>A
XM_017017220.1:c.2142+80T>A	XP_016872709.1:n.2142+80T>A
NM_001876.4:c.2142+80T>A MANE Select	NP_001867.2:n.2142+80T>A
NM_001031847.3:c.2142+80T>A	NP_001027017.1:n.2142+80T>A