Canonical Allele Identifier: CA13198369

Gene: LIPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88775030T>G , CM000672.2:g.88775030T>G	GRCh38
NC_000010.10:g.90534787T>G , CM000672.1:g.90534787T>G	GRCh37
NC_000010.9:g.90524767T>G	NCBI36
NG_031911.1:g.18625T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001102469.2:c.892-62T>G MANE Select	NP_001095939.1:n.892-62T>G
ENST00000404459.2:c.892-62T>G MANE Select	ENSP00000383923.1:n.892-62T>G
NM_001102469.1:c.892-62T>G	NP_001095939.1:n.892-62T>G
ENST00000404459.1:c.892-62T>G	ENSP00000383923.1:n.892-62T>G
XM_005270049.2:c.892-62T>G	XP_005270106.1:n.892-62T>G
XM_005270049.3:c.892-62T>G	XP_005270106.1:n.892-62T>G
XM_011540083.1:c.892-62T>G	XP_011538385.1:n.892-62T>G
XM_011540083.2:c.892-62T>G	XP_011538385.1:n.892-62T>G
XM_011540084.1:c.892-62T>G	XP_011538386.1:n.892-62T>G
XM_011540084.2:c.892-62T>G	XP_011538386.1:n.892-62T>G
XM_011540085.1:c.820-62T>G	XP_011538387.1:n.820-62T>G
XM_011540085.2:c.820-62T>G	XP_011538387.1:n.820-62T>G
XM_011540086.1:c.820-2979T>G	XP_011538388.1:n.820-2979T>G
XM_011540086.2:c.820-2979T>G	XP_011538388.1:n.820-2979T>G