Canonical Allele Identifier: CA6152698

Gene: CPT1A

Linked Data

• ClinVar Variation Id: 2911099
• ClinVar RCV Id: RCV003751402
• dbSNP Id: rs746957592
• ExAC: 11:68575028 G / A
• gnomAD v2: 11-68575028-G-A
• gnomAD v3: 11-68807560-G-A
• gnomAD v4: 11-68807560-G-A
• MyVariant Identifiers: chr11:g.68575028G>A (hg19) ; chr11:g.68807560G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68807560G>A , CM000673.2:g.68807560G>A	GRCh38
NC_000011.9:g.68575028G>A , CM000673.1:g.68575028G>A	GRCh37
NC_000011.8:g.68331604G>A	NCBI36
NG_011801.1:g.39372C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265641.10:c.360C>T MANE Select	ENSP00000265641.4:p.Val120=
ENST00000265641.9:c.360C>T	ENSP00000265641.4:p.Val120=
ENST00000376618.6:c.360C>T	ENSP00000365803.2:p.Val120=
ENST00000539743.5:c.360C>T	ENSP00000446108.1:p.Val120=
ENST00000540367.5:c.360C>T	ENSP00000439084.1:p.Val120=
ENST00000565318.5:c.360C>T	ENSP00000457826.1:p.Val120=
NM_001031847.2:c.360C>T	NP_001027017.1:p.Val120=
NM_001876.3:c.360C>T	NP_001867.2:p.Val120=
XM_005273762.1:c.456C>T	XP_005273819.1:p.Val152=
XM_005273763.1:c.456C>T	XP_005273820.1:p.Val152=
XM_005273762.3:c.456C>T	XP_005273819.1:p.Val152=
XM_017017220.1:c.360C>T	XP_016872709.1:p.Val120=
NM_001876.4:c.360C>T MANE Select	NP_001867.2:p.Val120=
NM_001031847.3:c.360C>T	NP_001027017.1:p.Val120=