Canonical Allele Identifier: CA166743519

Gene: LEP

Linked Data

• dbSNP Id: rs891433893
• MyVariant Identifiers: chr7:g.127887215G>A (hg19) ; chr7:g.128247162G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247162G>A , CM000669.2:g.128247162G>A	GRCh38
NC_000007.13:g.127887215G>A , CM000669.1:g.127887215G>A	GRCh37
NC_000007.12:g.127674451G>A	NCBI36
NG_007450.1:g.10885G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4829G>A MANE Select	ENSP00000312652.4:n.-28-4829G>A
ENST00000308868.4:c.-28-4829G>A	ENSP00000312652.4:n.-28-4829G>A
NM_000230.2:c.-28-4829G>A	NP_000221.1:n.-28-4829G>A
XM_005250340.3:c.-28-4829G>A	XP_005250397.1:n.-28-4829G>A
XM_005250340.5:c.-28-4829G>A	XP_005250397.1:n.-28-4829G>A
NM_000230.3:c.-28-4829G>A MANE Select	NP_000221.1:n.-28-4829G>A