Canonical Allele Identifier: CA223371829

Gene: CPT1A

Linked Data

• ClinVar Variation Id: 1516044
• ClinVar RCV Id: RCV002023655
• dbSNP Id: rs985269276
• MyVariant Identifiers: chr11:g.68542900A>C (hg19) ; chr11:g.68775432A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68775432A>C , CM000673.2:g.68775432A>C	GRCh38
NC_000011.9:g.68542900A>C , CM000673.1:g.68542900A>C	GRCh37
NC_000011.8:g.68299476A>C	NCBI36
NG_011801.1:g.71500T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.1459T>G MANE Select	ENSP00000265641.4:p.Tyr487Asp
ENST00000265641.9:c.1459T>G	ENSP00000265641.4:p.Tyr487Asp
ENST00000376618.6:c.1459T>G	ENSP00000365803.2:p.Tyr487Asp
ENST00000539743.5:c.1459T>G	ENSP00000446108.1:p.Tyr487Asp
ENST00000540367.5:c.1459T>G	ENSP00000439084.1:p.Tyr487Asp
NM_001031847.2:c.1459T>G	NP_001027017.1:p.Tyr487Asp
NM_001876.3:c.1459T>G	NP_001867.2:p.Tyr487Asp
XM_005273762.1:c.1555T>G	XP_005273819.1:p.Tyr519Asp
XM_005273763.1:c.1555T>G	XP_005273820.1:p.Tyr519Asp
XM_005273762.3:c.1555T>G	XP_005273819.1:p.Tyr519Asp
XM_017017220.1:c.1459T>G	XP_016872709.1:p.Tyr487Asp
NM_001876.4:c.1459T>G MANE Select	NP_001867.2:p.Tyr487Asp
NM_001031847.3:c.1459T>G	NP_001027017.1:p.Tyr487Asp