Canonical Allele Identifier: CA737948219

Gene: LEPR

Linked Data

• dbSNP Id: rs1157176769
• gnomAD v3: 1-65500750-T-G
• gnomAD v4: 1-65500750-T-G
• MyVariant Identifiers: chr1:g.65966433T>G (hg19) ; chr1:g.65500750T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65500750T>G , CM000663.2:g.65500750T>G	GRCh38
NC_000001.10:g.65966433T>G , CM000663.1:g.65966433T>G	GRCh37
NC_000001.9:g.65739021T>G	NCBI36
NG_015831.2:g.85186T>G , LRG_283:g.85186T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000349533.11:c.-20-64796T>G MANE Select	ENSP00000330393.7:n.-20-64796T>G
ENST00000349533.10:c.-20-64796T>G	ENSP00000330393.6:n.-20-64796T>G
ENST00000371059.7:c.-20-64796T>G	ENSP00000360098.3:n.-20-64796T>G
ENST00000371060.7:c.-20-64796T>G	ENSP00000360099.3:n.-20-64796T>G
ENST00000406510.7:c.-640-64796T>G	ENSP00000384025.3:n.-640-64796T>G
NM_001003679.3:c.-20-64796T>G , LRG_283t1:c.-20-64796T>G	NP_001003679.1:n.-20-64796T>G
NM_001003680.3:c.-20-64796T>G , LRG_283t2:c.-20-64796T>G	NP_001003680.1:n.-20-64796T>G
NM_002303.5:c.-20-64796T>G , LRG_283t3:c.-20-64796T>G	NP_002294.2:n.-20-64796T>G
NM_002303.6:c.-20-64796T>G MANE Select	NP_002294.2:n.-20-64796T>G