Canonical Allele Identifier: CA475205357

Gene: CPT1A

Linked Data

• MyVariant Identifiers: chr11:g.68571480G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68804012G>A , CM000673.2:g.68804012G>A	GRCh38
NC_000011.9:g.68571480G>A , CM000673.1:g.68571480G>A	GRCh37
NC_000011.8:g.68328056G>A	NCBI36
NG_011801.1:g.42920C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265641.10:c.543C>T MANE Select	ENSP00000265641.4:p.Asp181=
ENST00000265641.9:c.543C>T	ENSP00000265641.4:p.Asp181=
ENST00000376618.6:c.543C>T	ENSP00000365803.2:p.Asp181=
ENST00000539743.5:c.543C>T	ENSP00000446108.1:p.Asp181=
ENST00000540367.5:c.543C>T	ENSP00000439084.1:p.Asp181=
NM_001031847.2:c.543C>T	NP_001027017.1:p.Asp181=
NM_001876.3:c.543C>T	NP_001867.2:p.Asp181=
XM_005273762.1:c.639C>T	XP_005273819.1:p.Asp213=
XM_005273763.1:c.639C>T	XP_005273820.1:p.Asp213=
XM_005273762.3:c.639C>T	XP_005273819.1:p.Asp213=
XM_017017220.1:c.543C>T	XP_016872709.1:p.Asp181=
NM_001876.4:c.543C>T MANE Select	NP_001867.2:p.Asp181=
NM_001031847.3:c.543C>T	NP_001027017.1:p.Asp181=