Canonical Allele Identifier: CA381631942

Gene: CPT1A

Linked Data

• ClinVar Variation Id: 1055687
• ClinVar RCV Id: RCV001364399
• dbSNP Id: rs1451283997
• gnomAD v2: 11-68549408-G-A
• gnomAD v4: 11-68781940-G-A
• MyVariant Identifiers: chr11:g.68549408G>A (hg19) ; chr11:g.68781940G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68781940G>A , CM000673.2:g.68781940G>A	GRCh38
NC_000011.9:g.68549408G>A , CM000673.1:g.68549408G>A	GRCh37
NC_000011.8:g.68305984G>A	NCBI36
NG_011801.1:g.64992C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.1183C>T MANE Select	ENSP00000265641.4:p.Arg395Cys
ENST00000265641.9:c.1183C>T	ENSP00000265641.4:p.Arg395Cys
ENST00000376618.6:c.1183C>T	ENSP00000365803.2:p.Arg395Cys
ENST00000539743.5:c.1183C>T	ENSP00000446108.1:p.Arg395Cys
ENST00000540367.5:c.1183C>T	ENSP00000439084.1:p.Arg395Cys
NM_001031847.2:c.1183C>T	NP_001027017.1:p.Arg395Cys
NM_001876.3:c.1183C>T	NP_001867.2:p.Arg395Cys
XM_005273762.1:c.1279C>T	XP_005273819.1:p.Arg427Cys
XM_005273763.1:c.1279C>T	XP_005273820.1:p.Arg427Cys
XM_005273762.3:c.1279C>T	XP_005273819.1:p.Arg427Cys
XM_017017220.1:c.1183C>T	XP_016872709.1:p.Arg395Cys
NM_001876.4:c.1183C>T MANE Select	NP_001867.2:p.Arg395Cys
NM_001031847.3:c.1183C>T	NP_001027017.1:p.Arg395Cys