Canonical Allele Identifier: CA1172356575

Gene: LEPR

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349533.11:c.95G= MANE Select	ENSP00000330393.7:p.Arg32=
ENST00000344610.12:c.95G=	ENSP00000340884.8:p.Arg32=
ENST00000349533.10:c.95G=	ENSP00000330393.6:p.Arg32=
ENST00000371058.1:c.95G=	ENSP00000360097.1:p.Arg32=
ENST00000371059.7:c.95G=	ENSP00000360098.3:p.Arg32=
ENST00000371060.7:c.95G=	ENSP00000360099.3:p.Arg32=
ENST00000406510.7:c.-526G=	ENSP00000384025.3:n.-526G=
ENST00000462765.5:n.245G=
ENST00000616738.4:c.95G=	ENSP00000483390.1:p.Arg32=
NM_001003679.3:c.95G= , LRG_283t1:c.95G=	NP_001003679.1:p.Arg32=
NM_001003680.3:c.95G= , LRG_283t2:c.95G=	NP_001003680.1:p.Arg32=
NM_001198687.1:c.95G=	NP_001185616.1:p.Arg32=
NM_001198688.1:c.95G= , LRG_283t4:c.95G=	NP_001185617.1:p.Arg32=
NM_001198689.1:c.95G=	NP_001185618.1:p.Arg32=
NM_002303.5:c.95G= , LRG_283t3:c.95G=	NP_002294.2:p.Arg32=
NM_001198687.2:c.95G=	NP_001185616.1:p.Arg32=
NM_002303.6:c.95G= MANE Select	NP_002294.2:p.Arg32=
NM_001198689.2:c.95G=	NP_001185618.1:p.Arg32=