Canonical Allele Identifier: CA2715774829

Gene: LEP

Linked Data

• dbSNP Id: rs2116212605

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247331_128247344del , CM000669.2:g.128247331_128247344del	GRCh38
NC_000007.13:g.127887384_127887397del , CM000669.1:g.127887384_127887397del	GRCh37
NC_000007.12:g.127674620_127674633del	NCBI36
NG_007450.1:g.11054_11067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4660_-28-4647del MANE Select	ENSP00000312652.4:n.-28-4660_-28-4647del
ENST00000308868.4:c.-28-4660_-28-4647del	ENSP00000312652.4:n.-28-4660_-28-4647del
NM_000230.2:c.-28-4660_-28-4647del	NP_000221.1:n.-28-4660_-28-4647del
XM_005250340.3:c.-28-4660_-28-4647del	XP_005250397.1:n.-28-4660_-28-4647del
XM_005250340.5:c.-28-4660_-28-4647del	XP_005250397.1:n.-28-4660_-28-4647del
NM_000230.3:c.-28-4660_-28-4647del MANE Select	NP_000221.1:n.-28-4660_-28-4647del