Canonical Allele Identifier: CA1742265248

Gene: LEP

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247477C= , CM000669.2:g.128247477C=	GRCh38
NC_000007.13:g.127887530C= , CM000669.1:g.127887530C=	GRCh37
NC_000007.12:g.127674766C=	NCBI36
NG_007450.1:g.11200C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4514C= MANE Select	ENSP00000312652.4:n.-28-4514C=
ENST00000308868.4:c.-28-4514C=	ENSP00000312652.4:n.-28-4514C=
NM_000230.2:c.-28-4514C=	NP_000221.1:n.-28-4514C=
XM_005250340.3:c.-28-4514C=	XP_005250397.1:n.-28-4514C=
XM_005250340.5:c.-28-4514C=	XP_005250397.1:n.-28-4514C=
NM_000230.3:c.-28-4514C= MANE Select	NP_000221.1:n.-28-4514C=