Canonical Allele Identifier: CA1742266117

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128248581_128248582delinsAG , CM000669.2:g.128248581_128248582delinsAG	GRCh38
NC_000007.13:g.127888634_127888635delinsAG , CM000669.1:g.127888634_127888635delinsAG	GRCh37
NC_000007.12:g.127675870_127675871delinsAG	NCBI36
NG_007450.1:g.12304_12305delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-3410_-28-3409delinsAG MANE Select	ENSP00000312652.4:n.-28-3410_-28-3409delinsAG
ENST00000308868.4:c.-28-3410_-28-3409delinsAG	ENSP00000312652.4:n.-28-3410_-28-3409delinsAG
NM_000230.2:c.-28-3410_-28-3409delinsAG	NP_000221.1:n.-28-3410_-28-3409delinsAG
XM_005250340.3:c.-28-3410_-28-3409delinsAG	XP_005250397.1:n.-28-3410_-28-3409delinsAG
XM_005250340.5:c.-28-3410_-28-3409delinsAG	XP_005250397.1:n.-28-3410_-28-3409delinsAG
NM_000230.3:c.-28-3410_-28-3409delinsAG MANE Select	NP_000221.1:n.-28-3410_-28-3409delinsAG