Canonical Allele Identifier: CA594935209

Gene: LIPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88761795_88761802del , CM000672.2:g.88761795_88761802del	GRCh38
NC_000010.10:g.90521552_90521559del , CM000672.1:g.90521552_90521559del	GRCh37
NC_000010.9:g.90511532_90511539del	NCBI36
NG_031911.1:g.5390_5397del

Transcript Alleles

HGVS	Amino-acid Change
NM_001102469.2:c.108+282_108+289del MANE Select	NP_001095939.1:n.108+282_108+289del
ENST00000404459.2:c.108+282_108+289del MANE Select	ENSP00000383923.1:n.108+282_108+289del
NM_001102469.1:c.108+282_108+289del	NP_001095939.1:n.108+282_108+289del
ENST00000404459.1:c.108+282_108+289del	ENSP00000383923.1:n.108+282_108+289del
ENST00000674982.1:n.241+282_241+289del
XM_005270049.2:c.108+282_108+289del	XP_005270106.1:n.108+282_108+289del
XM_005270049.3:c.108+282_108+289del	XP_005270106.1:n.108+282_108+289del
XM_011540083.1:c.108+282_108+289del	XP_011538385.1:n.108+282_108+289del
XM_011540083.2:c.108+282_108+289del	XP_011538385.1:n.108+282_108+289del
XM_011540084.1:c.108+282_108+289del	XP_011538386.1:n.108+282_108+289del
XM_011540084.2:c.108+282_108+289del	XP_011538386.1:n.108+282_108+289del
XM_011540085.1:c.108+282_108+289del	XP_011538387.1:n.108+282_108+289del
XM_011540085.2:c.108+282_108+289del	XP_011538387.1:n.108+282_108+289del
XM_011540086.1:c.108+282_108+289del	XP_011538388.1:n.108+282_108+289del
XM_011540086.2:c.108+282_108+289del	XP_011538388.1:n.108+282_108+289del
XM_017016549.1:c.108+282_108+289del	XP_016872038.1:n.108+282_108+289del
XR_945801.1:n.437+282_437+289del