Canonical Allele Identifier: CA1742271753

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128254578C= , CM000669.2:g.128254578C=	GRCh38
NC_000007.13:g.127894631C= , CM000669.1:g.127894631C=	GRCh37
NC_000007.12:g.127681867C=	NCBI36
NG_007450.1:g.18301C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000308868.5:c.319C= MANE Select	ENSP00000312652.4:p.Leu107=
ENST00000308868.4:c.319C=	ENSP00000312652.4:p.Leu107=
NM_000230.2:c.319C=	NP_000221.1:p.Leu107=
XM_005250340.3:c.316C=	XP_005250397.1:p.Leu106=
XM_005250340.5:c.316C=	XP_005250397.1:p.Leu106=
NM_000230.3:c.319C= MANE Select	NP_000221.1:p.Leu107=