Canonical Allele Identifier: CA833092074

Gene: LEP

Linked Data

• dbSNP Id: rs1402357698
• MyVariant Identifiers: chr7:g.127887322del (hg19) ; chr7:g.128247269del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247271del , CM000669.2:g.128247271del	GRCh38
NC_000007.13:g.127887324del , CM000669.1:g.127887324del	GRCh37
NC_000007.12:g.127674560del	NCBI36
NG_007450.1:g.10994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4720del MANE Select	ENSP00000312652.4:n.-28-4720del
ENST00000308868.4:c.-28-4720del	ENSP00000312652.4:n.-28-4720del
NM_000230.2:c.-28-4720del	NP_000221.1:n.-28-4720del
XM_005250340.3:c.-28-4720del	XP_005250397.1:n.-28-4720del
XM_005250340.5:c.-28-4720del	XP_005250397.1:n.-28-4720del
NM_000230.3:c.-28-4720del MANE Select	NP_000221.1:n.-28-4720del