Canonical Allele Identifier: CA381637958
Gene: CPT1A HGNC NCBI

Linked Data

dbSNP Id: rs747227699

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68812486C>G , CM000673.2:g.68812486C>G GRCh38
NC_000011.9:g.68579954C>G , CM000673.1:g.68579954C>G GRCh37
NC_000011.8:g.68336530C>G NCBI36
NG_011801.1:g.34446G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265641.10:c.232G>C MANE Select ENSP00000265641.4:p.Asp78His
ENST00000265641.9:c.232G>C ENSP00000265641.4:p.Asp78His
ENST00000376618.6:c.232G>C ENSP00000365803.2:p.Asp78His
ENST00000539743.5:c.232G>C ENSP00000446108.1:p.Asp78His
ENST00000540367.5:c.232G>C ENSP00000439084.1:p.Asp78His
ENST00000561996.1:c.232G>C ENSP00000457663.1:p.Asp78His
ENST00000565318.5:c.232G>C ENSP00000457826.1:p.Asp78His
ENST00000569129.5:c.232G>C ENSP00000455116.1:p.Asp78His
NM_001031847.2:c.232G>C NP_001027017.1:p.Asp78His
NM_001876.3:c.232G>C NP_001867.2:p.Asp78His
XM_005273762.1:c.328G>C XP_005273819.1:p.Asp110His
XM_005273763.1:c.328G>C XP_005273820.1:p.Asp110His
XM_005273762.3:c.328G>C XP_005273819.1:p.Asp110His
XM_017017220.1:c.232G>C XP_016872709.1:p.Asp78His
NM_001876.4:c.232G>C MANE Select NP_001867.2:p.Asp78His
NM_001031847.3:c.232G>C NP_001027017.1:p.Asp78His