Canonical Allele Identifier: CA2672449889
Gene: LRAT HGNC NCBI

Linked Data

gnomAD v4: 4-154751602-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154751602C>A , CM000666.2:g.154751602C>A GRCh38
NC_000004.11:g.155672754C>A , CM000666.1:g.155672754C>A GRCh37
NC_000004.10:g.155892204C>A NCBI36
NG_009110.1:g.12592C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336356.4:c.*2466C>A MANE Select ENSP00000337224.3:n.*2466C>A
ENST00000336356.3:c.*2466C>A ENSP00000337224.3:n.*2466C>A
ENST00000510733.1:n.3486C>A
NM_001301645.1:c.*2466C>A NP_001288574.1:n.*2466C>A
NM_004744.4:c.*2466C>A NP_004735.2:n.*2466C>A
NM_004744.5:c.*2466C>A MANE Select NP_004735.2:n.*2466C>A
NM_001301645.2:c.*2466C>A NP_001288574.1:n.*2466C>A
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