Canonical Allele Identifier: CA1742265158

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247356G= , CM000669.2:g.128247356G=	GRCh38
NC_000007.13:g.127887409G= , CM000669.1:g.127887409G=	GRCh37
NC_000007.12:g.127674645G=	NCBI36
NG_007450.1:g.11079G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4635G= MANE Select	ENSP00000312652.4:n.-28-4635G=
ENST00000308868.4:c.-28-4635G=	ENSP00000312652.4:n.-28-4635G=
NM_000230.2:c.-28-4635G=	NP_000221.1:n.-28-4635G=
XM_005250340.3:c.-28-4635G=	XP_005250397.1:n.-28-4635G=
XM_005250340.5:c.-28-4635G=	XP_005250397.1:n.-28-4635G=
NM_000230.3:c.-28-4635G= MANE Select	NP_000221.1:n.-28-4635G=