Canonical Allele Identifier: CA1742266274

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128248787_128248788delinsTG , CM000669.2:g.128248787_128248788delinsTG	GRCh38
NC_000007.13:g.127888840_127888841delinsTG , CM000669.1:g.127888840_127888841delinsTG	GRCh37
NC_000007.12:g.127676076_127676077delinsTG	NCBI36
NG_007450.1:g.12510_12511delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-3204_-28-3203delinsTG MANE Select	ENSP00000312652.4:n.-28-3204_-28-3203delinsTG
ENST00000308868.4:c.-28-3204_-28-3203delinsTG	ENSP00000312652.4:n.-28-3204_-28-3203delinsTG
NM_000230.2:c.-28-3204_-28-3203delinsTG	NP_000221.1:n.-28-3204_-28-3203delinsTG
XM_005250340.3:c.-28-3204_-28-3203delinsTG	XP_005250397.1:n.-28-3204_-28-3203delinsTG
XM_005250340.5:c.-28-3204_-28-3203delinsTG	XP_005250397.1:n.-28-3204_-28-3203delinsTG
NM_000230.3:c.-28-3204_-28-3203delinsTG MANE Select	NP_000221.1:n.-28-3204_-28-3203delinsTG