Canonical Allele Identifier: CA1742265171

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247363_128247364delinsCA , CM000669.2:g.128247363_128247364delinsCA	GRCh38
NC_000007.13:g.127887416_127887417delinsCA , CM000669.1:g.127887416_127887417delinsCA	GRCh37
NC_000007.12:g.127674652_127674653delinsCA	NCBI36
NG_007450.1:g.11086_11087delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4628_-28-4627delinsCA MANE Select	ENSP00000312652.4:n.-28-4628_-28-4627delinsCA
ENST00000308868.4:c.-28-4628_-28-4627delinsCA	ENSP00000312652.4:n.-28-4628_-28-4627delinsCA
NM_000230.2:c.-28-4628_-28-4627delinsCA	NP_000221.1:n.-28-4628_-28-4627delinsCA
XM_005250340.3:c.-28-4628_-28-4627delinsCA	XP_005250397.1:n.-28-4628_-28-4627delinsCA
XM_005250340.5:c.-28-4628_-28-4627delinsCA	XP_005250397.1:n.-28-4628_-28-4627delinsCA
NM_000230.3:c.-28-4628_-28-4627delinsCA MANE Select	NP_000221.1:n.-28-4628_-28-4627delinsCA