Canonical Allele Identifier: CA3026359837

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2917042A>T , CM000680.2:g.2917042A>T	GRCh38
NC_000018.9:g.2917040A>T , CM000680.1:g.2917040A>T	GRCh37
NC_000018.8:g.2907040A>T	NCBI36
NG_007507.1:g.99906T>A , LRG_174:g.99906T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001375808.2:c.*3251T>A MANE Select	NP_001362737.1:n.*3251T>A
ENST00000677752.1:c.*3251T>A MANE Select	ENSP00000504857.1:n.*3251T>A
NM_001375808.1:c.*3251T>A	NP_001362737.1:n.*3251T>A
NM_001375809.1:c.*3251T>A	NP_001362738.1:n.*3251T>A
NM_014646.2:c.*3251T>A , LRG_174t1:c.*3251T>A	NP_055461.1:n.*3251T>A
ENST00000261596.8:c.*3251T>A	ENSP00000261596.4:n.*3251T>A
ENST00000261596.9:c.*3251T>A	ENSP00000261596.4:n.*3251T>A
ENST00000697039.1:c.2546+3736T>A	ENSP00000513061.1:n.2546+3736T>A
ENST00000697040.1:c.*3251T>A	ENSP00000513062.1:n.*3251T>A
XM_005258177.3:c.*3251T>A	XP_005258234.1:n.*3251T>A
XM_005258177.4:c.*3251T>A	XP_005258234.1:n.*3251T>A
XM_005258178.2:c.*3251T>A	XP_005258235.1:n.*3251T>A
XM_005258178.3:c.*3251T>A	XP_005258235.1:n.*3251T>A
XM_005258179.3:c.*3251T>A	XP_005258236.1:n.*3251T>A
XM_005258179.5:c.*3251T>A	XP_005258236.1:n.*3251T>A
XM_017026098.1:c.*3251T>A	XP_016881587.1:n.*3251T>A
XM_017026099.1:c.*3251T>A	XP_016881588.1:n.*3251T>A