Canonical Allele Identifier: CA418436036
Gene: LEPR HGNC NCBI

Linked Data

gnomAD v4: 1-65570762-A-G
MyVariant Identifiers: chr1:g.66036445A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65570762A>G , CM000663.2:g.65570762A>G GRCh38
NC_000001.10:g.66036445A>G , CM000663.1:g.66036445A>G GRCh37
NC_000001.9:g.65809033A>G NCBI36
NG_015831.2:g.155198A>G , LRG_283:g.155198A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000349533.11:c.330A>G MANE Select ENSP00000330393.7:p.Thr110=
ENST00000344610.12:c.330A>G ENSP00000340884.8:p.Thr110=
ENST00000349533.10:c.330A>G ENSP00000330393.6:p.Thr110=
ENST00000371058.1:c.330A>G ENSP00000360097.1:p.Thr110=
ENST00000371059.7:c.330A>G ENSP00000360098.3:p.Thr110=
ENST00000371060.7:c.330A>G ENSP00000360099.3:p.Thr110=
ENST00000406510.7:c.-291A>G ENSP00000384025.3:n.-291A>G
ENST00000462765.5:n.480A>G
ENST00000616738.4:c.330A>G ENSP00000483390.1:p.Thr110=
NM_001003679.3:c.330A>G , LRG_283t1:c.330A>G NP_001003679.1:p.Thr110=
NM_001003680.3:c.330A>G , LRG_283t2:c.330A>G NP_001003680.1:p.Thr110=
NM_001198687.1:c.330A>G NP_001185616.1:p.Thr110=
NM_001198688.1:c.330A>G , LRG_283t4:c.330A>G NP_001185617.1:p.Thr110=
NM_001198689.1:c.330A>G NP_001185618.1:p.Thr110=
NM_002303.5:c.330A>G , LRG_283t3:c.330A>G NP_002294.2:p.Thr110=
NM_001198687.2:c.330A>G NP_001185616.1:p.Thr110=
NM_002303.6:c.330A>G MANE Select NP_002294.2:p.Thr110=
NM_001198689.2:c.330A>G NP_001185618.1:p.Thr110=