Canonical Allele Identifier: CA1139848029

Gene: LEPR LEPROT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.65432298G= , CM000663.2:g.65432298G=	GRCh38
NC_000001.10:g.65897981G= , CM000663.1:g.65897981G=	GRCh37
NC_000001.9:g.65670569G=	NCBI36
NG_015831.2:g.16734G= , LRG_283:g.16734G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002303.6:c.-21+6920G= (LEPR) MANE Select	NP_002294.2:n.-21+6920G=
NM_017526.5:c.*379G= (LEPROT) MANE Select	NP_059996.1:n.*379G=
ENST00000349533.11:c.-21+6920G= (LEPR) MANE Select	ENSP00000330393.7:n.-21+6920G=
ENST00000371065.9:c.*379G= (LEPROT) MANE Select	ENSP00000360104.4:n.*379G=
NM_001003679.3:c.-21+6920G= , LRG_283t1:c.-21+6920G= (LEPR)	NP_001003679.1:n.-21+6920G=
NM_001003680.3:c.-21+6920G= , LRG_283t2:c.-21+6920G= (LEPR)	NP_001003680.1:n.-21+6920G=
NM_001198681.1:c.*379G= (LEPROT)	NP_001185610.1:n.*379G=
NM_001198681.2:c.*379G= (LEPROT)	NP_001185610.1:n.*379G=
NM_002303.5:c.-21+6920G= , LRG_283t3:c.-21+6920G= (LEPR)	NP_002294.2:n.-21+6920G=
NM_017526.4:c.*379G= (LEPROT)	NP_059996.1:n.*379G=
ENST00000349533.10:c.-21+6920G= (LEPR)	ENSP00000330393.6:n.-21+6920G=
ENST00000371059.7:c.-21+6920G= (LEPR)	ENSP00000360098.3:n.-21+6920G=
ENST00000371060.7:c.-21+6920G= (LEPR)	ENSP00000360099.3:n.-21+6920G=
ENST00000371065.8:c.*379G= (LEPROT)	ENSP00000360104.4:n.*379G=
ENST00000406510.7:c.-641+6920G= (LEPR)	ENSP00000384025.3:n.-641+6920G=
ENST00000613538.1:c.*379G= (LEPROT)	ENSP00000483521.1:n.*379G=