Canonical Allele Identifier: CA475207562

Gene: CPT1A

Linked Data

• MyVariant Identifiers: chr11:g.68580015T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68812547T>G , CM000673.2:g.68812547T>G	GRCh38
NC_000011.9:g.68580015T>G , CM000673.1:g.68580015T>G	GRCh37
NC_000011.8:g.68336591T>G	NCBI36
NG_011801.1:g.34385A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265641.10:c.171A>C MANE Select	ENSP00000265641.4:p.Ala57=
ENST00000265641.9:c.171A>C	ENSP00000265641.4:p.Ala57=
ENST00000376618.6:c.171A>C	ENSP00000365803.2:p.Ala57=
ENST00000539743.5:c.171A>C	ENSP00000446108.1:p.Ala57=
ENST00000540367.5:c.171A>C	ENSP00000439084.1:p.Ala57=
ENST00000561996.1:c.171A>C	ENSP00000457663.1:p.Ala57=
ENST00000565318.5:c.171A>C	ENSP00000457826.1:p.Ala57=
ENST00000569129.5:c.171A>C	ENSP00000455116.1:p.Ala57=
NM_001031847.2:c.171A>C	NP_001027017.1:p.Ala57=
NM_001876.3:c.171A>C	NP_001867.2:p.Ala57=
XM_005273762.1:c.267A>C	XP_005273819.1:p.Ala89=
XM_005273763.1:c.267A>C	XP_005273820.1:p.Ala89=
XM_005273762.3:c.267A>C	XP_005273819.1:p.Ala89=
XM_017017220.1:c.171A>C	XP_016872709.1:p.Ala57=
NM_001876.4:c.171A>C MANE Select	NP_001867.2:p.Ala57=
NM_001031847.3:c.171A>C	NP_001027017.1:p.Ala57=