Canonical Allele Identifier: CA6152059
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1978287
ClinVar RCV Id: RCV002741757
dbSNP Id: rs762300383

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68759655C>T , CM000673.2:g.68759655C>T GRCh38
NC_000011.9:g.68527123C>T , CM000673.1:g.68527123C>T GRCh37
NC_000011.8:g.68283699C>T NCBI36
NG_011801.1:g.87277G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265641.10:c.2149G>A MANE Select ENSP00000265641.4:p.Asp717Asn
ENST00000265641.9:c.2149G>A ENSP00000265641.4:p.Asp717Asn
ENST00000376618.6:c.2149G>A ENSP00000365803.2:p.Asp717Asn
ENST00000539743.5:c.2149G>A ENSP00000446108.1:p.Asp717Asn
ENST00000540367.5:c.2149G>A ENSP00000439084.1:p.Asp717Asn
NM_001031847.2:c.2149G>A NP_001027017.1:p.Asp717Asn
NM_001876.3:c.2149G>A NP_001867.2:p.Asp717Asn
XM_005273762.1:c.2245G>A XP_005273819.1:p.Asp749Asn
XM_005273763.1:c.2245G>A XP_005273820.1:p.Asp749Asn
XM_005273762.3:c.2245G>A XP_005273819.1:p.Asp749Asn
XM_017017220.1:c.2149G>A XP_016872709.1:p.Asp717Asn
NM_001876.4:c.2149G>A MANE Select NP_001867.2:p.Asp717Asn
NM_001031847.3:c.2149G>A NP_001027017.1:p.Asp717Asn