Canonical Allele Identifier: CA2280791490
Gene: LPIN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2929075T= , CM000680.2:g.2929075T= GRCh38
NC_000018.9:g.2929073T= , CM000680.1:g.2929073T= GRCh37
NC_000018.8:g.2919073T= NCBI36
NG_007507.1:g.87873A= , LRG_174:g.87873A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261596.9:c.1540A= ENSP00000261596.4:p.Ile514=
ENST00000697039.1:c.1540A= ENSP00000513061.1:p.Ile514=
ENST00000697040.1:c.1540A= ENSP00000513062.1:p.Ile514=
ENST00000697041.1:c.235A= ENSP00000513063.1:p.Ile79=
ENST00000697042.1:c.1540A= ENSP00000513064.1:p.Ile514=
ENST00000677752.1:c.1540A= MANE Select ENSP00000504857.1:p.Ile514=
ENST00000261596.8:c.1540A= ENSP00000261596.4:p.Ile514=
NM_014646.2:c.1540A= , LRG_174t1:c.1540A= NP_055461.1:p.Ile514=
XM_005258177.3:c.1651A= XP_005258234.1:p.Ile551=
XM_005258178.2:c.1540A= XP_005258235.1:p.Ile514=
XM_005258179.3:c.1540A= XP_005258236.1:p.Ile514=
XR_935074.1:n.1669A=
XM_005258177.4:c.1651A= XP_005258234.1:p.Ile551=
XM_005258178.3:c.1540A= XP_005258235.1:p.Ile514=
XM_005258179.5:c.1540A= XP_005258236.1:p.Ile514=
XM_017026098.1:c.1540A= XP_016881587.1:p.Ile514=
XM_017026099.1:c.1540A= XP_016881588.1:p.Ile514=
XR_935074.2:n.1714A=
NM_001375808.1:c.1540A= NP_001362737.1:p.Ile514=
NM_001375809.1:c.1540A= NP_001362738.1:p.Ile514=
NM_001375808.2:c.1540A= MANE Select NP_001362737.1:p.Ile514=