Canonical Allele Identifier: CA8873226

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2937814G>C , CM000680.2:g.2937814G>C	GRCh38
NC_000018.9:g.2937812G>C , CM000680.1:g.2937812G>C	GRCh37
NC_000018.8:g.2927812G>C	NCBI36
NG_007507.1:g.79134C>G , LRG_174:g.79134C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261596.9:c.1046C>G	ENSP00000261596.4:p.Pro349Arg
ENST00000697039.1:c.1046C>G	ENSP00000513061.1:p.Pro349Arg
ENST00000697040.1:c.1046C>G	ENSP00000513062.1:p.Pro349Arg
ENST00000697042.1:c.1046C>G	ENSP00000513064.1:p.Pro349Arg
ENST00000677752.1:c.1046C>G MANE Select	ENSP00000504857.1:p.Pro349Arg
ENST00000261596.8:c.1046C>G	ENSP00000261596.4:p.Pro349Arg
NM_014646.2:c.1046C>G , LRG_174t1:c.1046C>G	NP_055461.1:p.Pro349Arg
XM_005258177.3:c.1157C>G	XP_005258234.1:p.Pro386Arg
XM_005258178.2:c.1046C>G	XP_005258235.1:p.Pro349Arg
XM_005258179.3:c.1046C>G	XP_005258236.1:p.Pro349Arg
XR_935074.1:n.1175C>G
XM_005258177.4:c.1157C>G	XP_005258234.1:p.Pro386Arg
XM_005258178.3:c.1046C>G	XP_005258235.1:p.Pro349Arg
XM_005258179.5:c.1046C>G	XP_005258236.1:p.Pro349Arg
XM_017026098.1:c.1046C>G	XP_016881587.1:p.Pro349Arg
XM_017026099.1:c.1046C>G	XP_016881588.1:p.Pro349Arg
XR_935074.2:n.1220C>G
NM_001375808.1:c.1046C>G	NP_001362737.1:p.Pro349Arg
NM_001375809.1:c.1046C>G	NP_001362738.1:p.Pro349Arg
NM_001375808.2:c.1046C>G MANE Select	NP_001362737.1:p.Pro349Arg