Canonical Allele Identifier: CA1172377285
Gene: LEPR HGNC NCBI

Linked Data

dbSNP Id: rs1657978984

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.65623040_65623041insTGAAAATGTGAACAGTTA , CM000663.2:g.65623040_65623041insTGAAAATGTGAACAGTTA GRCh38
NC_000001.10:g.66088723_66088724insTGAAAATGTGAACAGTTA , CM000663.1:g.66088723_66088724insTGAAAATGTGAACAGTTA GRCh37
NC_000001.9:g.65861311_65861312insTGAAAATGTGAACAGTTA NCBI36
NG_015831.2:g.207476_207477insTGAAAATGTGAACAGTTA , LRG_283:g.207476_207477insTGAAAATGTGAACAGTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000349533.11:c.2673+59_2673+60insTGAAAATGTGAACAGTTA MANE Select ENSP00000330393.7:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
ENST00000344610.12:c.2673+59_2673+60insTGAAAATGTGAACAGTTA ENSP00000340884.8:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
ENST00000349533.10:c.2673+59_2673+60insTGAAAATGTGAACAGTTA ENSP00000330393.6:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
ENST00000371058.1:c.2673+59_2673+60insTGAAAATGTGAACAGTTA ENSP00000360097.1:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
ENST00000371059.7:c.2673+59_2673+60insTGAAAATGTGAACAGTTA ENSP00000360098.3:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
ENST00000371060.7:c.2673+59_2673+60insTGAAAATGTGAACAGTTA ENSP00000360099.3:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
ENST00000406510.7:c.-126-13151_-126-13150insTGAAAATGTGAACAGTTA ENSP00000384025.3:n.-126-13151_-126-13150insTGAAAATGTGAACAGTT...
ENST00000471762.1:n.325_326insTGAAAATGTGAACAGTTA
ENST00000616738.4:c.2673+59_2673+60insTGAAAATGTGAACAGTTA ENSP00000483390.1:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
NM_001003679.3:c.2673+59_2673+60insTGAAAATGTGAACAGTTA , LRG_283t1:c.2673+59_2673+60insTGAAAATGTGAACAGTTA NP_001003679.1:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
NM_001003680.3:c.2673+59_2673+60insTGAAAATGTGAACAGTTA , LRG_283t2:c.2673+59_2673+60insTGAAAATGTGAACAGTTA NP_001003680.1:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
NM_001198687.1:c.2673+59_2673+60insTGAAAATGTGAACAGTTA NP_001185616.1:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
NM_001198688.1:c.2673+59_2673+60insTGAAAATGTGAACAGTTA , LRG_283t4:c.2673+59_2673+60insTGAAAATGTGAACAGTTA NP_001185617.1:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
NM_001198689.1:c.2673+59_2673+60insTGAAAATGTGAACAGTTA NP_001185618.1:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
NM_002303.5:c.2673+59_2673+60insTGAAAATGTGAACAGTTA , LRG_283t3:c.2673+59_2673+60insTGAAAATGTGAACAGTTA NP_002294.2:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
NM_001198687.2:c.2673+59_2673+60insTGAAAATGTGAACAGTTA NP_001185616.1:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
NM_002303.6:c.2673+59_2673+60insTGAAAATGTGAACAGTTA MANE Select NP_002294.2:n.2673+59_2673+60insTGAAAATGTGAACAGTTA
NM_001198689.2:c.2673+59_2673+60insTGAAAATGTGAACAGTTA NP_001185618.1:n.2673+59_2673+60insTGAAAATGTGAACAGTTA