Canonical Allele Identifier: CA16041536
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 371151
ClinVar RCV Id: RCV001037328
dbSNP Id: rs1057517046

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68775433C>T , CM000673.2:g.68775433C>T GRCh38
NC_000011.9:g.68542901C>T , CM000673.1:g.68542901C>T GRCh37
NC_000011.8:g.68299477C>T NCBI36
NG_011801.1:g.71499G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265641.10:c.1459-1G>A MANE Select ENSP00000265641.4:n.1459-1G>A
ENST00000265641.9:c.1459-1G>A ENSP00000265641.4:n.1459-1G>A
ENST00000376618.6:c.1459-1G>A ENSP00000365803.2:n.1459-1G>A
ENST00000539743.5:c.1459-1G>A ENSP00000446108.1:n.1459-1G>A
ENST00000540367.5:c.1459-1G>A ENSP00000439084.1:n.1459-1G>A
NM_001031847.2:c.1459-1G>A NP_001027017.1:n.1459-1G>A
NM_001876.3:c.1459-1G>A NP_001867.2:n.1459-1G>A
XM_005273762.1:c.1555-1G>A XP_005273819.1:n.1555-1G>A
XM_005273763.1:c.1555-1G>A XP_005273820.1:n.1555-1G>A
XM_005273762.3:c.1555-1G>A XP_005273819.1:n.1555-1G>A
XM_017017220.1:c.1459-1G>A XP_016872709.1:n.1459-1G>A
NM_001876.4:c.1459-1G>A MANE Select NP_001867.2:n.1459-1G>A
NM_001031847.3:c.1459-1G>A NP_001027017.1:n.1459-1G>A