Canonical Allele Identifier: CA401706617

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2937892G>A , CM000680.2:g.2937892G>A	GRCh38
NC_000018.9:g.2937890G>A , CM000680.1:g.2937890G>A	GRCh37
NC_000018.8:g.2927890G>A	NCBI36
NG_007507.1:g.79056C>T , LRG_174:g.79056C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261596.9:c.968C>T	ENSP00000261596.4:p.Thr323Ile
ENST00000697039.1:c.968C>T	ENSP00000513061.1:p.Thr323Ile
ENST00000697040.1:c.968C>T	ENSP00000513062.1:p.Thr323Ile
ENST00000697042.1:c.968C>T	ENSP00000513064.1:p.Thr323Ile
ENST00000677752.1:c.968C>T MANE Select	ENSP00000504857.1:p.Thr323Ile
ENST00000261596.8:c.968C>T	ENSP00000261596.4:p.Thr323Ile
NM_014646.2:c.968C>T , LRG_174t1:c.968C>T	NP_055461.1:p.Thr323Ile
XM_005258177.3:c.1079C>T	XP_005258234.1:p.Thr360Ile
XM_005258178.2:c.968C>T	XP_005258235.1:p.Thr323Ile
XM_005258179.3:c.968C>T	XP_005258236.1:p.Thr323Ile
XR_935074.1:n.1097C>T
XM_005258177.4:c.1079C>T	XP_005258234.1:p.Thr360Ile
XM_005258178.3:c.968C>T	XP_005258235.1:p.Thr323Ile
XM_005258179.5:c.968C>T	XP_005258236.1:p.Thr323Ile
XM_017026098.1:c.968C>T	XP_016881587.1:p.Thr323Ile
XM_017026099.1:c.968C>T	XP_016881588.1:p.Thr323Ile
XR_935074.2:n.1142C>T
NM_001375808.1:c.968C>T	NP_001362737.1:p.Thr323Ile
NM_001375809.1:c.968C>T	NP_001362738.1:p.Thr323Ile
NM_001375808.2:c.968C>T MANE Select	NP_001362737.1:p.Thr323Ile