Canonical Allele Identifier: CA358629850
Community Standard Title: NM_004744.5(LRAT):c.40G>T (p.Glu14Ter)
Gene: LRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154744366G>T , CM000666.2:g.154744366G>T GRCh38
NC_000004.11:g.155665518G>T , CM000666.1:g.155665518G>T GRCh37
NC_000004.10:g.155884968G>T NCBI36
NG_009110.1:g.5356G>T

Transcript Alleles

HGVS Amino-acid Change
NM_004744.5:c.40G>T MANE Select NP_004735.2:p.Glu14Ter
ENST00000336356.4:c.40G>T MANE Select ENSP00000337224.3:p.Glu14Ter
NM_001301645.1:c.40G>T NP_001288574.1:p.Glu14Ter
NM_001301645.2:c.40G>T NP_001288574.1:p.Glu14Ter
NM_004744.4:c.40G>T NP_004735.2:p.Glu14Ter
ENST00000336356.3:c.40G>T ENSP00000337224.3:p.Glu14Ter
ENST00000499392.1:n.472-3823G>T
ENST00000502525.5:c.40G>T ENSP00000422324.1:p.Glu14Ter
ENST00000507827.5:c.40G>T ENSP00000426761.1:p.Glu14Ter
ENST00000510733.1:n.367G>T
XM_006714412.2:c.40G>T XP_006714475.1:p.Glu14Ter
XR_938793.1:n.376G>T
XR_938793.2:n.372G>T