Canonical Allele Identifier: CA1742266276

Gene: LEP

Linked Data

• dbSNP Id: rs1795243111

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128248788del , CM000669.2:g.128248788del	GRCh38
NC_000007.13:g.127888841del , CM000669.1:g.127888841del	GRCh37
NC_000007.12:g.127676077del	NCBI36
NG_007450.1:g.12511del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-3203del MANE Select	ENSP00000312652.4:n.-28-3203del
ENST00000308868.4:c.-28-3203del	ENSP00000312652.4:n.-28-3203del
NM_000230.2:c.-28-3203del	NP_000221.1:n.-28-3203del
XM_005250340.3:c.-28-3203del	XP_005250397.1:n.-28-3203del
XM_005250340.5:c.-28-3203del	XP_005250397.1:n.-28-3203del
NM_000230.3:c.-28-3203del MANE Select	NP_000221.1:n.-28-3203del