Canonical Allele Identifier: CA1742266237

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128248723_128248724delinsAG , CM000669.2:g.128248723_128248724delinsAG	GRCh38
NC_000007.13:g.127888776_127888777delinsAG , CM000669.1:g.127888776_127888777delinsAG	GRCh37
NC_000007.12:g.127676012_127676013delinsAG	NCBI36
NG_007450.1:g.12446_12447delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-3268_-28-3267delinsAG MANE Select	ENSP00000312652.4:n.-28-3268_-28-3267delinsAG
ENST00000308868.4:c.-28-3268_-28-3267delinsAG	ENSP00000312652.4:n.-28-3268_-28-3267delinsAG
NM_000230.2:c.-28-3268_-28-3267delinsAG	NP_000221.1:n.-28-3268_-28-3267delinsAG
XM_005250340.3:c.-28-3268_-28-3267delinsAG	XP_005250397.1:n.-28-3268_-28-3267delinsAG
XM_005250340.5:c.-28-3268_-28-3267delinsAG	XP_005250397.1:n.-28-3268_-28-3267delinsAG
NM_000230.3:c.-28-3268_-28-3267delinsAG MANE Select	NP_000221.1:n.-28-3268_-28-3267delinsAG