Canonical Allele Identifier: CA1742265242

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247466_128247467delinsGC , CM000669.2:g.128247466_128247467delinsGC	GRCh38
NC_000007.13:g.127887519_127887520delinsGC , CM000669.1:g.127887519_127887520delinsGC	GRCh37
NC_000007.12:g.127674755_127674756delinsGC	NCBI36
NG_007450.1:g.11189_11190delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4525_-28-4524delinsGC MANE Select	ENSP00000312652.4:n.-28-4525_-28-4524delinsGC
ENST00000308868.4:c.-28-4525_-28-4524delinsGC	ENSP00000312652.4:n.-28-4525_-28-4524delinsGC
NM_000230.2:c.-28-4525_-28-4524delinsGC	NP_000221.1:n.-28-4525_-28-4524delinsGC
XM_005250340.3:c.-28-4525_-28-4524delinsGC	XP_005250397.1:n.-28-4525_-28-4524delinsGC
XM_005250340.5:c.-28-4525_-28-4524delinsGC	XP_005250397.1:n.-28-4525_-28-4524delinsGC
NM_000230.3:c.-28-4525_-28-4524delinsGC MANE Select	NP_000221.1:n.-28-4525_-28-4524delinsGC