Canonical Allele Identifier: CA340671992
Gene: LEPR HGNC NCBI

Linked Data

dbSNP Id: rs1360127522
gnomAD v2: 1-66036210-G-T
gnomAD v4: 1-65570527-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65570527G>T , CM000663.2:g.65570527G>T GRCh38
NC_000001.10:g.66036210G>T , CM000663.1:g.66036210G>T GRCh37
NC_000001.9:g.65808798G>T NCBI36
NG_015831.2:g.154963G>T , LRG_283:g.154963G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000349533.11:c.95G>T MANE Select ENSP00000330393.7:p.Arg32Ile
ENST00000344610.12:c.95G>T ENSP00000340884.8:p.Arg32Ile
ENST00000349533.10:c.95G>T ENSP00000330393.6:p.Arg32Ile
ENST00000371058.1:c.95G>T ENSP00000360097.1:p.Arg32Ile
ENST00000371059.7:c.95G>T ENSP00000360098.3:p.Arg32Ile
ENST00000371060.7:c.95G>T ENSP00000360099.3:p.Arg32Ile
ENST00000406510.7:c.-526G>T ENSP00000384025.3:n.-526G>T
ENST00000462765.5:n.245G>T
ENST00000616738.4:c.95G>T ENSP00000483390.1:p.Arg32Ile
NM_001003679.3:c.95G>T , LRG_283t1:c.95G>T NP_001003679.1:p.Arg32Ile
NM_001003680.3:c.95G>T , LRG_283t2:c.95G>T NP_001003680.1:p.Arg32Ile
NM_001198687.1:c.95G>T NP_001185616.1:p.Arg32Ile
NM_001198688.1:c.95G>T , LRG_283t4:c.95G>T NP_001185617.1:p.Arg32Ile
NM_001198689.1:c.95G>T NP_001185618.1:p.Arg32Ile
NM_002303.5:c.95G>T , LRG_283t3:c.95G>T NP_002294.2:p.Arg32Ile
NM_001198687.2:c.95G>T NP_001185616.1:p.Arg32Ile
NM_002303.6:c.95G>T MANE Select NP_002294.2:p.Arg32Ile
NM_001198689.2:c.95G>T NP_001185618.1:p.Arg32Ile