Canonical Allele Identifier: CA166743869

Gene: LEP

Linked Data

• dbSNP Id: rs964241686
• MyVariant Identifiers: chr7:g.127888665T>A (hg19) ; chr7:g.128248612T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128248612T>A , CM000669.2:g.128248612T>A	GRCh38
NC_000007.13:g.127888665T>A , CM000669.1:g.127888665T>A	GRCh37
NC_000007.12:g.127675901T>A	NCBI36
NG_007450.1:g.12335T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-3379T>A MANE Select	ENSP00000312652.4:n.-28-3379T>A
ENST00000308868.4:c.-28-3379T>A	ENSP00000312652.4:n.-28-3379T>A
NM_000230.2:c.-28-3379T>A	NP_000221.1:n.-28-3379T>A
XM_005250340.3:c.-28-3379T>A	XP_005250397.1:n.-28-3379T>A
XM_005250340.5:c.-28-3379T>A	XP_005250397.1:n.-28-3379T>A
NM_000230.3:c.-28-3379T>A MANE Select	NP_000221.1:n.-28-3379T>A