Canonical Allele Identifier: CA894493

Gene: LEPR

Linked Data

• dbSNP Id: rs765458310
• ExAC: 1:66036381 G / T
• gnomAD v2: 1-66036381-G-T
• gnomAD v3: 1-65570698-G-T
• gnomAD v4: 1-65570698-G-T
• MyVariant Identifiers: chr1:g.66036381G>T (hg19) ; chr1:g.65570698G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65570698G>T , CM000663.2:g.65570698G>T	GRCh38
NC_000001.10:g.66036381G>T , CM000663.1:g.66036381G>T	GRCh37
NC_000001.9:g.65808969G>T	NCBI36
NG_015831.2:g.155134G>T , LRG_283:g.155134G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349533.11:c.266G>T MANE Select	ENSP00000330393.7:p.Cys89Phe
ENST00000344610.12:c.266G>T	ENSP00000340884.8:p.Cys89Phe
ENST00000349533.10:c.266G>T	ENSP00000330393.6:p.Cys89Phe
ENST00000371058.1:c.266G>T	ENSP00000360097.1:p.Cys89Phe
ENST00000371059.7:c.266G>T	ENSP00000360098.3:p.Cys89Phe
ENST00000371060.7:c.266G>T	ENSP00000360099.3:p.Cys89Phe
ENST00000406510.7:c.-355G>T	ENSP00000384025.3:n.-355G>T
ENST00000462765.5:n.416G>T
ENST00000616738.4:c.266G>T	ENSP00000483390.1:p.Cys89Phe
NM_001003679.3:c.266G>T , LRG_283t1:c.266G>T	NP_001003679.1:p.Cys89Phe
NM_001003680.3:c.266G>T , LRG_283t2:c.266G>T	NP_001003680.1:p.Cys89Phe
NM_001198687.1:c.266G>T	NP_001185616.1:p.Cys89Phe
NM_001198688.1:c.266G>T , LRG_283t4:c.266G>T	NP_001185617.1:p.Cys89Phe
NM_001198689.1:c.266G>T	NP_001185618.1:p.Cys89Phe
NM_002303.5:c.266G>T , LRG_283t3:c.266G>T	NP_002294.2:p.Cys89Phe
NM_001198687.2:c.266G>T	NP_001185616.1:p.Cys89Phe
NM_002303.6:c.266G>T MANE Select	NP_002294.2:p.Cys89Phe
NM_001198689.2:c.266G>T	NP_001185618.1:p.Cys89Phe