Canonical Allele Identifier: CA2640829384

Gene: LPIN2

Linked Data

• gnomAD v4: 18-2928979-G-GAACACTTTTATAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2928992_2928993insCAACACTTTTATAA , CM000680.2:g.2928992_2928993insCAACACTTTTATAA	GRCh38
NC_000018.9:g.2928990_2928991insCAACACTTTTATAA , CM000680.1:g.2928990_2928991insCAACACTTTTATAA	GRCh37
NC_000018.8:g.2918990_2918991insCAACACTTTTATAA	NCBI36
NG_007507.1:g.87968_87969insGTTATAAAAGTGTT , LRG_174:g.87968_87969insGTTATAAAAGTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261596.9:c.1550+85_1550+86insGTTATAAAAGTGTT	ENSP00000261596.4:n.1550+85_1550+86insGTTATAAAAGTGTT
ENST00000697039.1:c.1550+85_1550+86insGTTATAAAAGTGTT	ENSP00000513061.1:n.1550+85_1550+86insGTTATAAAAGTGTT
ENST00000697040.1:c.1550+85_1550+86insGTTATAAAAGTGTT	ENSP00000513062.1:n.1550+85_1550+86insGTTATAAAAGTGTT
ENST00000697041.1:c.245+85_245+86insGTTATAAAAGTGTT	ENSP00000513063.1:n.245+85_245+86insGTTATAAAAGTGTT
ENST00000697042.1:c.1550+85_1550+86insGTTATAAAAGTGTT	ENSP00000513064.1:n.1550+85_1550+86insGTTATAAAAGTGTT
ENST00000677752.1:c.1550+85_1550+86insGTTATAAAAGTGTT MANE Select	ENSP00000504857.1:n.1550+85_1550+86insGTTATAAAAGTGTT
ENST00000261596.8:c.1550+85_1550+86insGTTATAAAAGTGTT	ENSP00000261596.4:n.1550+85_1550+86insGTTATAAAAGTGTT
NM_014646.2:c.1550+85_1550+86insGTTATAAAAGTGTT , LRG_174t1:c.1550+85_1550+86insGTTATAAAAGTGTT	NP_055461.1:n.1550+85_1550+86insGTTATAAAAGTGTT
XM_005258177.3:c.1661+85_1661+86insGTTATAAAAGTGTT	XP_005258234.1:n.1661+85_1661+86insGTTATAAAAGTGTT
XM_005258178.2:c.1550+85_1550+86insGTTATAAAAGTGTT	XP_005258235.1:n.1550+85_1550+86insGTTATAAAAGTGTT
XM_005258179.3:c.1550+85_1550+86insGTTATAAAAGTGTT	XP_005258236.1:n.1550+85_1550+86insGTTATAAAAGTGTT
XR_935074.1:n.1679+85_1679+86insGTTATAAAAGTGTT
XM_005258177.4:c.1661+85_1661+86insGTTATAAAAGTGTT	XP_005258234.1:n.1661+85_1661+86insGTTATAAAAGTGTT
XM_005258178.3:c.1550+85_1550+86insGTTATAAAAGTGTT	XP_005258235.1:n.1550+85_1550+86insGTTATAAAAGTGTT
XM_005258179.5:c.1550+85_1550+86insGTTATAAAAGTGTT	XP_005258236.1:n.1550+85_1550+86insGTTATAAAAGTGTT
XM_017026098.1:c.1550+85_1550+86insGTTATAAAAGTGTT	XP_016881587.1:n.1550+85_1550+86insGTTATAAAAGTGTT
XM_017026099.1:c.1550+85_1550+86insGTTATAAAAGTGTT	XP_016881588.1:n.1550+85_1550+86insGTTATAAAAGTGTT
XR_935074.2:n.1724+85_1724+86insGTTATAAAAGTGTT
NM_001375808.1:c.1550+85_1550+86insGTTATAAAAGTGTT	NP_001362737.1:n.1550+85_1550+86insGTTATAAAAGTGTT
NM_001375809.1:c.1550+85_1550+86insGTTATAAAAGTGTT	NP_001362738.1:n.1550+85_1550+86insGTTATAAAAGTGTT
NM_001375808.2:c.1550+85_1550+86insGTTATAAAAGTGTT MANE Select	NP_001362737.1:n.1550+85_1550+86insGTTATAAAAGTGTT