Canonical Allele Identifier: CA2672448468

Gene: LRAT

Linked Data

• gnomAD v4: 4-154744696-G-GTCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744700_154744703dup , CM000666.2:g.154744700_154744703dup	GRCh38
NC_000004.11:g.155665852_155665855dup , CM000666.1:g.155665852_155665855dup	GRCh37
NC_000004.10:g.155885302_155885305dup	NCBI36
NG_009110.1:g.5690_5693dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.374_377dup MANE Select	ENSP00000337224.3:p.His126GlnfsTer22
ENST00000336356.3:c.374_377dup	ENSP00000337224.3:p.His126GlnfsTer22
ENST00000499392.1:n.472-3489_472-3486dup
ENST00000507827.5:c.374_377dup	ENSP00000426761.1:p.His126GlnfsTer22
ENST00000510733.1:n.701_704dup
NM_001301645.1:c.374_377dup	NP_001288574.1:p.His126GlnfsTer22
NM_004744.4:c.374_377dup	NP_004735.2:p.His126GlnfsTer22
XM_006714412.2:c.374_377dup	XP_006714475.1:p.His126GlnfsTer22
XR_938793.1:n.710_713dup
XR_938793.2:n.706_709dup
NM_004744.5:c.374_377dup MANE Select	NP_004735.2:p.His126GlnfsTer22
NM_001301645.2:c.374_377dup	NP_001288574.1:p.His126GlnfsTer22