Canonical Allele Identifier: CA418436050

Gene: LEPR

Linked Data

• MyVariant Identifiers: chr1:g.66036451T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65570768T>G , CM000663.2:g.65570768T>G	GRCh38
NC_000001.10:g.66036451T>G , CM000663.1:g.66036451T>G	GRCh37
NC_000001.9:g.65809039T>G	NCBI36
NG_015831.2:g.155204T>G , LRG_283:g.155204T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000349533.11:c.336T>G MANE Select	ENSP00000330393.7:p.Val112=
ENST00000344610.12:c.336T>G	ENSP00000340884.8:p.Val112=
ENST00000349533.10:c.336T>G	ENSP00000330393.6:p.Val112=
ENST00000371058.1:c.336T>G	ENSP00000360097.1:p.Val112=
ENST00000371059.7:c.336T>G	ENSP00000360098.3:p.Val112=
ENST00000371060.7:c.336T>G	ENSP00000360099.3:p.Val112=
ENST00000406510.7:c.-285T>G	ENSP00000384025.3:n.-285T>G
ENST00000462765.5:n.486T>G
ENST00000616738.4:c.336T>G	ENSP00000483390.1:p.Val112=
NM_001003679.3:c.336T>G , LRG_283t1:c.336T>G	NP_001003679.1:p.Val112=
NM_001003680.3:c.336T>G , LRG_283t2:c.336T>G	NP_001003680.1:p.Val112=
NM_001198687.1:c.336T>G	NP_001185616.1:p.Val112=
NM_001198688.1:c.336T>G , LRG_283t4:c.336T>G	NP_001185617.1:p.Val112=
NM_001198689.1:c.336T>G	NP_001185618.1:p.Val112=
NM_002303.5:c.336T>G , LRG_283t3:c.336T>G	NP_002294.2:p.Val112=
NM_001198687.2:c.336T>G	NP_001185616.1:p.Val112=
NM_002303.6:c.336T>G MANE Select	NP_002294.2:p.Val112=
NM_001198689.2:c.336T>G	NP_001185618.1:p.Val112=