Canonical Allele Identifier: CA1742265221

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247441T= , CM000669.2:g.128247441T=	GRCh38
NC_000007.13:g.127887494T= , CM000669.1:g.127887494T=	GRCh37
NC_000007.12:g.127674730T=	NCBI36
NG_007450.1:g.11164T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4550T= MANE Select	ENSP00000312652.4:n.-28-4550T=
ENST00000308868.4:c.-28-4550T=	ENSP00000312652.4:n.-28-4550T=
NM_000230.2:c.-28-4550T=	NP_000221.1:n.-28-4550T=
XM_005250340.3:c.-28-4550T=	XP_005250397.1:n.-28-4550T=
XM_005250340.5:c.-28-4550T=	XP_005250397.1:n.-28-4550T=
NM_000230.3:c.-28-4550T= MANE Select	NP_000221.1:n.-28-4550T=