Canonical Allele Identifier: CA381636034

Gene: CPT1A

Linked Data

• MyVariant Identifiers: chr11:g.68571517G>C (hg19) ; chr11:g.68804049G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68804049G>C , CM000673.2:g.68804049G>C	GRCh38
NC_000011.9:g.68571517G>C , CM000673.1:g.68571517G>C	GRCh37
NC_000011.8:g.68328093G>C	NCBI36
NG_011801.1:g.42883C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.506C>G MANE Select	ENSP00000265641.4:p.Thr169Arg
ENST00000265641.9:c.506C>G	ENSP00000265641.4:p.Thr169Arg
ENST00000376618.6:c.506C>G	ENSP00000365803.2:p.Thr169Arg
ENST00000539743.5:c.506C>G	ENSP00000446108.1:p.Thr169Arg
ENST00000540367.5:c.506C>G	ENSP00000439084.1:p.Thr169Arg
NM_001031847.2:c.506C>G	NP_001027017.1:p.Thr169Arg
NM_001876.3:c.506C>G	NP_001867.2:p.Thr169Arg
XM_005273762.1:c.602C>G	XP_005273819.1:p.Thr201Arg
XM_005273763.1:c.602C>G	XP_005273820.1:p.Thr201Arg
XM_005273762.3:c.602C>G	XP_005273819.1:p.Thr201Arg
XM_017017220.1:c.506C>G	XP_016872709.1:p.Thr169Arg
NM_001876.4:c.506C>G MANE Select	NP_001867.2:p.Thr169Arg
NM_001031847.3:c.506C>G	NP_001027017.1:p.Thr169Arg