Canonical Allele Identifier: CA778216695

Gene: LPIN2

Linked Data

• dbSNP Id: rs1410638323
• gnomAD v3: 18-2928966-G-A
• gnomAD v4: 18-2928966-G-A
• MyVariant Identifiers: chr18:g.2928964G>A (hg19) ; chr18:g.2928966G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2928966G>A , CM000680.2:g.2928966G>A	GRCh38
NC_000018.9:g.2928964G>A , CM000680.1:g.2928964G>A	GRCh37
NC_000018.8:g.2918964G>A	NCBI36
NG_007507.1:g.87982C>T , LRG_174:g.87982C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261596.9:c.1550+99C>T	ENSP00000261596.4:n.1550+99C>T
ENST00000697039.1:c.1550+99C>T	ENSP00000513061.1:n.1550+99C>T
ENST00000697040.1:c.1550+99C>T	ENSP00000513062.1:n.1550+99C>T
ENST00000697041.1:c.245+99C>T	ENSP00000513063.1:n.245+99C>T
ENST00000697042.1:c.1550+99C>T	ENSP00000513064.1:n.1550+99C>T
ENST00000677752.1:c.1550+99C>T MANE Select	ENSP00000504857.1:n.1550+99C>T
ENST00000261596.8:c.1550+99C>T	ENSP00000261596.4:n.1550+99C>T
NM_014646.2:c.1550+99C>T , LRG_174t1:c.1550+99C>T	NP_055461.1:n.1550+99C>T
XM_005258177.3:c.1661+99C>T	XP_005258234.1:n.1661+99C>T
XM_005258178.2:c.1550+99C>T	XP_005258235.1:n.1550+99C>T
XM_005258179.3:c.1550+99C>T	XP_005258236.1:n.1550+99C>T
XR_935074.1:n.1679+99C>T
XM_005258177.4:c.1661+99C>T	XP_005258234.1:n.1661+99C>T
XM_005258178.3:c.1550+99C>T	XP_005258235.1:n.1550+99C>T
XM_005258179.5:c.1550+99C>T	XP_005258236.1:n.1550+99C>T
XM_017026098.1:c.1550+99C>T	XP_016881587.1:n.1550+99C>T
XM_017026099.1:c.1550+99C>T	XP_016881588.1:n.1550+99C>T
XR_935074.2:n.1724+99C>T
NM_001375808.1:c.1550+99C>T	NP_001362737.1:n.1550+99C>T
NM_001375809.1:c.1550+99C>T	NP_001362738.1:n.1550+99C>T
NM_001375808.2:c.1550+99C>T MANE Select	NP_001362737.1:n.1550+99C>T