Canonical Allele Identifier: CA381634668

Gene: CPT1A

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68794881G>A , CM000673.2:g.68794881G>A	GRCh38
NC_000011.9:g.68562349G>A , CM000673.1:g.68562349G>A	GRCh37
NC_000011.8:g.68318925G>A	NCBI36
NG_011801.1:g.52051C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.802C>T MANE Select	ENSP00000265641.4:p.Gln268Ter
ENST00000265641.9:c.802C>T	ENSP00000265641.4:p.Gln268Ter
ENST00000376618.6:c.802C>T	ENSP00000365803.2:p.Gln268Ter
ENST00000538994.1:c.58C>T	ENSP00000454332.1:p.Gln20Ter
ENST00000539743.5:c.802C>T	ENSP00000446108.1:p.Gln268Ter
ENST00000540367.5:c.802C>T	ENSP00000439084.1:p.Gln268Ter
NM_001031847.2:c.802C>T	NP_001027017.1:p.Gln268Ter
NM_001876.3:c.802C>T	NP_001867.2:p.Gln268Ter
XM_005273762.1:c.898C>T	XP_005273819.1:p.Gln300Ter
XM_005273763.1:c.898C>T	XP_005273820.1:p.Gln300Ter
XM_005273762.3:c.898C>T	XP_005273819.1:p.Gln300Ter
XM_017017220.1:c.802C>T	XP_016872709.1:p.Gln268Ter
NM_001876.4:c.802C>T MANE Select	NP_001867.2:p.Gln268Ter
NM_001031847.3:c.802C>T	NP_001027017.1:p.Gln268Ter