Canonical Allele Identifier: CA2640829402

Gene: LPIN2

Linked Data

• gnomAD v4: 18-2928999-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2928999G>T , CM000680.2:g.2928999G>T	GRCh38
NC_000018.9:g.2928997G>T , CM000680.1:g.2928997G>T	GRCh37
NC_000018.8:g.2918997G>T	NCBI36
NG_007507.1:g.87949C>A , LRG_174:g.87949C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261596.9:c.1550+66C>A	ENSP00000261596.4:n.1550+66C>A
ENST00000697039.1:c.1550+66C>A	ENSP00000513061.1:n.1550+66C>A
ENST00000697040.1:c.1550+66C>A	ENSP00000513062.1:n.1550+66C>A
ENST00000697041.1:c.245+66C>A	ENSP00000513063.1:n.245+66C>A
ENST00000697042.1:c.1550+66C>A	ENSP00000513064.1:n.1550+66C>A
ENST00000677752.1:c.1550+66C>A MANE Select	ENSP00000504857.1:n.1550+66C>A
ENST00000261596.8:c.1550+66C>A	ENSP00000261596.4:n.1550+66C>A
NM_014646.2:c.1550+66C>A , LRG_174t1:c.1550+66C>A	NP_055461.1:n.1550+66C>A
XM_005258177.3:c.1661+66C>A	XP_005258234.1:n.1661+66C>A
XM_005258178.2:c.1550+66C>A	XP_005258235.1:n.1550+66C>A
XM_005258179.3:c.1550+66C>A	XP_005258236.1:n.1550+66C>A
XR_935074.1:n.1679+66C>A
XM_005258177.4:c.1661+66C>A	XP_005258234.1:n.1661+66C>A
XM_005258178.3:c.1550+66C>A	XP_005258235.1:n.1550+66C>A
XM_005258179.5:c.1550+66C>A	XP_005258236.1:n.1550+66C>A
XM_017026098.1:c.1550+66C>A	XP_016881587.1:n.1550+66C>A
XM_017026099.1:c.1550+66C>A	XP_016881588.1:n.1550+66C>A
XR_935074.2:n.1724+66C>A
NM_001375808.1:c.1550+66C>A	NP_001362737.1:n.1550+66C>A
NM_001375809.1:c.1550+66C>A	NP_001362738.1:n.1550+66C>A
NM_001375808.2:c.1550+66C>A MANE Select	NP_001362737.1:n.1550+66C>A