Canonical Allele Identifier: CA1107007399

Gene: LEP

Linked Data

• dbSNP Id: rs1795223740
• gnomAD v3: 7-128247371-T-G
• gnomAD v4: 7-128247371-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247371T>G , CM000669.2:g.128247371T>G	GRCh38
NC_000007.13:g.127887424T>G , CM000669.1:g.127887424T>G	GRCh37
NC_000007.12:g.127674660T>G	NCBI36
NG_007450.1:g.11094T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4620T>G MANE Select	ENSP00000312652.4:n.-28-4620T>G
ENST00000308868.4:c.-28-4620T>G	ENSP00000312652.4:n.-28-4620T>G
NM_000230.2:c.-28-4620T>G	NP_000221.1:n.-28-4620T>G
XM_005250340.3:c.-28-4620T>G	XP_005250397.1:n.-28-4620T>G
XM_005250340.5:c.-28-4620T>G	XP_005250397.1:n.-28-4620T>G
NM_000230.3:c.-28-4620T>G MANE Select	NP_000221.1:n.-28-4620T>G