Canonical Allele Identifier: CA1742265099

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247292A= , CM000669.2:g.128247292A=	GRCh38
NC_000007.13:g.127887345A= , CM000669.1:g.127887345A=	GRCh37
NC_000007.12:g.127674581A=	NCBI36
NG_007450.1:g.11015A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4699A= MANE Select	ENSP00000312652.4:n.-28-4699A=
ENST00000308868.4:c.-28-4699A=	ENSP00000312652.4:n.-28-4699A=
NM_000230.2:c.-28-4699A=	NP_000221.1:n.-28-4699A=
XM_005250340.3:c.-28-4699A=	XP_005250397.1:n.-28-4699A=
XM_005250340.5:c.-28-4699A=	XP_005250397.1:n.-28-4699A=
NM_000230.3:c.-28-4699A= MANE Select	NP_000221.1:n.-28-4699A=