Canonical Allele Identifier: CA442020477

Gene: LRAT

Linked Data

• dbSNP Id: rs1385528380
• gnomAD v2: 4-155666006-C-G
• gnomAD v4: 4-154744854-C-G
• MyVariant Identifiers: chr4:g.155666006C>G (hg19) ; chr4:g.154744854C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154744854C>G , CM000666.2:g.154744854C>G	GRCh38
NC_000004.11:g.155666006C>G , CM000666.1:g.155666006C>G	GRCh37
NC_000004.10:g.155885456C>G	NCBI36
NG_009110.1:g.5844C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336356.4:c.528C>G MANE Select	ENSP00000337224.3:p.Pro176=
ENST00000336356.3:c.528C>G	ENSP00000337224.3:p.Pro176=
ENST00000499392.1:n.472-3335C>G
ENST00000507827.5:c.528C>G	ENSP00000426761.1:p.Pro176=
ENST00000510733.1:n.855C>G
NM_001301645.1:c.528C>G	NP_001288574.1:p.Pro176=
NM_004744.4:c.528C>G	NP_004735.2:p.Pro176=
XM_006714412.2:c.528C>G	XP_006714475.1:p.Pro176=
XR_938793.1:n.864C>G
XR_938793.2:n.860C>G
NM_004744.5:c.528C>G MANE Select	NP_004735.2:p.Pro176=
NM_001301645.2:c.528C>G	NP_001288574.1:p.Pro176=