Canonical Allele Identifier: CA166743860

Gene: LEP

Linked Data

• dbSNP Id: rs891038624
• gnomAD v2: 7-127888579-G-A
• gnomAD v3: 7-128248526-G-A
• gnomAD v4: 7-128248526-G-A
• MyVariant Identifiers: chr7:g.127888579G>A (hg19) ; chr7:g.128248526G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128248526G>A , CM000669.2:g.128248526G>A	GRCh38
NC_000007.13:g.127888579G>A , CM000669.1:g.127888579G>A	GRCh37
NC_000007.12:g.127675815G>A	NCBI36
NG_007450.1:g.12249G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-3465G>A MANE Select	ENSP00000312652.4:n.-28-3465G>A
ENST00000308868.4:c.-28-3465G>A	ENSP00000312652.4:n.-28-3465G>A
NM_000230.2:c.-28-3465G>A	NP_000221.1:n.-28-3465G>A
XM_005250340.3:c.-28-3465G>A	XP_005250397.1:n.-28-3465G>A
XM_005250340.5:c.-28-3465G>A	XP_005250397.1:n.-28-3465G>A
NM_000230.3:c.-28-3465G>A MANE Select	NP_000221.1:n.-28-3465G>A