Canonical Allele Identifier: CA223371851
Gene: CPT1A HGNC NCBI

Linked Data

dbSNP Id: rs565151030

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68775468G>T , CM000673.2:g.68775468G>T GRCh38
NC_000011.9:g.68542936G>T , CM000673.1:g.68542936G>T GRCh37
NC_000011.8:g.68299512G>T NCBI36
NG_011801.1:g.71464C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265641.10:c.1459-36C>A MANE Select ENSP00000265641.4:n.1459-36C>A
ENST00000265641.9:c.1459-36C>A ENSP00000265641.4:n.1459-36C>A
ENST00000376618.6:c.1459-36C>A ENSP00000365803.2:n.1459-36C>A
ENST00000539743.5:c.1459-36C>A ENSP00000446108.1:n.1459-36C>A
ENST00000540367.5:c.1459-36C>A ENSP00000439084.1:n.1459-36C>A
NM_001031847.2:c.1459-36C>A NP_001027017.1:n.1459-36C>A
NM_001876.3:c.1459-36C>A NP_001867.2:n.1459-36C>A
XM_005273762.1:c.1555-36C>A XP_005273819.1:n.1555-36C>A
XM_005273763.1:c.1555-36C>A XP_005273820.1:n.1555-36C>A
XM_005273762.3:c.1555-36C>A XP_005273819.1:n.1555-36C>A
XM_017017220.1:c.1459-36C>A XP_016872709.1:n.1459-36C>A
NM_001876.4:c.1459-36C>A MANE Select NP_001867.2:n.1459-36C>A
NM_001031847.3:c.1459-36C>A NP_001027017.1:n.1459-36C>A