Canonical Allele Identifier: CA918126072

Gene: LEP

Linked Data

• dbSNP Id: rs1562931025

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128248603del , CM000669.2:g.128248603del	GRCh38
NC_000007.13:g.127888656del , CM000669.1:g.127888656del	GRCh37
NC_000007.12:g.127675892del	NCBI36
NG_007450.1:g.12326del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-3388del MANE Select	ENSP00000312652.4:n.-28-3388del
ENST00000308868.4:c.-28-3388del	ENSP00000312652.4:n.-28-3388del
NM_000230.2:c.-28-3388del	NP_000221.1:n.-28-3388del
XM_005250340.3:c.-28-3388del	XP_005250397.1:n.-28-3388del
XM_005250340.5:c.-28-3388del	XP_005250397.1:n.-28-3388del
NM_000230.3:c.-28-3388del MANE Select	NP_000221.1:n.-28-3388del