Canonical Allele Identifier: CA3115885
Community Standard Title: NM_004744.5(LRAT):c.519G>T (p.Pro173=)
Gene: LRAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154744845G>T , CM000666.2:g.154744845G>T GRCh38
NC_000004.11:g.155665997G>T , CM000666.1:g.155665997G>T GRCh37
NC_000004.10:g.155885447G>T NCBI36
NG_009110.1:g.5835G>T

Transcript Alleles

HGVS Amino-acid Change
NM_004744.5:c.519G>T MANE Select NP_004735.2:p.Pro173=
ENST00000336356.4:c.519G>T MANE Select ENSP00000337224.3:p.Pro173=
NM_001301645.1:c.519G>T NP_001288574.1:p.Pro173=
NM_001301645.2:c.519G>T NP_001288574.1:p.Pro173=
NM_004744.4:c.519G>T NP_004735.2:p.Pro173=
ENST00000336356.3:c.519G>T ENSP00000337224.3:p.Pro173=
ENST00000499392.1:n.472-3344G>T
ENST00000507827.5:c.519G>T ENSP00000426761.1:p.Pro173=
ENST00000510733.1:n.846G>T
XM_006714412.2:c.519G>T XP_006714475.1:p.Pro173=
XR_938793.1:n.855G>T
XR_938793.2:n.851G>T