Canonical Allele Identifier: CA1742265243

Gene: LEP

Linked Data

• dbSNP Id: rs1795225077

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247467del , CM000669.2:g.128247467del	GRCh38
NC_000007.13:g.127887520del , CM000669.1:g.127887520del	GRCh37
NC_000007.12:g.127674756del	NCBI36
NG_007450.1:g.11190del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4524del MANE Select	ENSP00000312652.4:n.-28-4524del
ENST00000308868.4:c.-28-4524del	ENSP00000312652.4:n.-28-4524del
NM_000230.2:c.-28-4524del	NP_000221.1:n.-28-4524del
XM_005250340.3:c.-28-4524del	XP_005250397.1:n.-28-4524del
XM_005250340.5:c.-28-4524del	XP_005250397.1:n.-28-4524del
NM_000230.3:c.-28-4524del MANE Select	NP_000221.1:n.-28-4524del