Canonical Allele Identifier: CA1742264938

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247080_128247081delinsCA , CM000669.2:g.128247080_128247081delinsCA	GRCh38
NC_000007.13:g.127887133_127887134delinsCA , CM000669.1:g.127887133_127887134delinsCA	GRCh37
NC_000007.12:g.127674369_127674370delinsCA	NCBI36
NG_007450.1:g.10803_10804delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4911_-28-4910delinsCA MANE Select	ENSP00000312652.4:n.-28-4911_-28-4910delinsCA
ENST00000308868.4:c.-28-4911_-28-4910delinsCA	ENSP00000312652.4:n.-28-4911_-28-4910delinsCA
NM_000230.2:c.-28-4911_-28-4910delinsCA	NP_000221.1:n.-28-4911_-28-4910delinsCA
XM_005250340.3:c.-28-4911_-28-4910delinsCA	XP_005250397.1:n.-28-4911_-28-4910delinsCA
XM_005250340.5:c.-28-4911_-28-4910delinsCA	XP_005250397.1:n.-28-4911_-28-4910delinsCA
NM_000230.3:c.-28-4911_-28-4910delinsCA MANE Select	NP_000221.1:n.-28-4911_-28-4910delinsCA