Canonical Allele Identifier: CA381635202

Gene: CPT1A

Linked Data

• MyVariant Identifiers: chr11:g.68566701C>A (hg19) ; chr11:g.68799233C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68799233C>A , CM000673.2:g.68799233C>A	GRCh38
NC_000011.9:g.68566701C>A , CM000673.1:g.68566701C>A	GRCh37
NC_000011.8:g.68323277C>A	NCBI36
NG_011801.1:g.47699G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.678G>T MANE Select	ENSP00000265641.4:p.Trp226Cys
ENST00000265641.9:c.678G>T	ENSP00000265641.4:p.Trp226Cys
ENST00000376618.6:c.678G>T	ENSP00000365803.2:p.Trp226Cys
ENST00000538994.1:c.-67G>T	ENSP00000454332.1:n.-67G>T
ENST00000539743.5:c.678G>T	ENSP00000446108.1:p.Trp226Cys
ENST00000540367.5:c.678G>T	ENSP00000439084.1:p.Trp226Cys
NM_001031847.2:c.678G>T	NP_001027017.1:p.Trp226Cys
NM_001876.3:c.678G>T	NP_001867.2:p.Trp226Cys
XM_005273762.1:c.774G>T	XP_005273819.1:p.Trp258Cys
XM_005273763.1:c.774G>T	XP_005273820.1:p.Trp258Cys
XM_005273762.3:c.774G>T	XP_005273819.1:p.Trp258Cys
XM_017017220.1:c.678G>T	XP_016872709.1:p.Trp226Cys
NM_001876.4:c.678G>T MANE Select	NP_001867.2:p.Trp226Cys
NM_001031847.3:c.678G>T	NP_001027017.1:p.Trp226Cys