Canonical Allele Identifier: CA5591856

Gene: LIPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88764655A>T , CM000672.2:g.88764655A>T	GRCh38
NC_000010.10:g.90524412A>T , CM000672.1:g.90524412A>T	GRCh37
NC_000010.9:g.90514392A>T	NCBI36
NG_031911.1:g.8250A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001102469.2:c.425+47A>T MANE Select	NP_001095939.1:n.425+47A>T
ENST00000404459.2:c.425+47A>T MANE Select	ENSP00000383923.1:n.425+47A>T
NM_001102469.1:c.425+47A>T	NP_001095939.1:n.425+47A>T
ENST00000404459.1:c.425+47A>T	ENSP00000383923.1:n.425+47A>T
ENST00000674982.1:n.605A>T
XM_005270049.2:c.425+47A>T	XP_005270106.1:n.425+47A>T
XM_005270049.3:c.425+47A>T	XP_005270106.1:n.425+47A>T
XM_011540083.1:c.425+47A>T	XP_011538385.1:n.425+47A>T
XM_011540083.2:c.425+47A>T	XP_011538385.1:n.425+47A>T
XM_011540084.1:c.425+47A>T	XP_011538386.1:n.425+47A>T
XM_011540084.2:c.425+47A>T	XP_011538386.1:n.425+47A>T
XM_011540085.1:c.425+47A>T	XP_011538387.1:n.425+47A>T
XM_011540085.2:c.425+47A>T	XP_011538387.1:n.425+47A>T
XM_011540086.1:c.425+47A>T	XP_011538388.1:n.425+47A>T
XM_011540086.2:c.425+47A>T	XP_011538388.1:n.425+47A>T
XM_017016549.1:c.425+47A>T	XP_016872038.1:n.425+47A>T
XR_945801.1:n.754+47A>T