Canonical Allele Identifier: CA2280791445
Gene: LPIN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2928971A= , CM000680.2:g.2928971A= GRCh38
NC_000018.9:g.2928969A= , CM000680.1:g.2928969A= GRCh37
NC_000018.8:g.2918969A= NCBI36
NG_007507.1:g.87977T= , LRG_174:g.87977T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261596.9:c.1550+94T= ENSP00000261596.4:n.1550+94T=
ENST00000697039.1:c.1550+94T= ENSP00000513061.1:n.1550+94T=
ENST00000697040.1:c.1550+94T= ENSP00000513062.1:n.1550+94T=
ENST00000697041.1:c.245+94T= ENSP00000513063.1:n.245+94T=
ENST00000697042.1:c.1550+94T= ENSP00000513064.1:n.1550+94T=
ENST00000677752.1:c.1550+94T= MANE Select ENSP00000504857.1:n.1550+94T=
ENST00000261596.8:c.1550+94T= ENSP00000261596.4:n.1550+94T=
NM_014646.2:c.1550+94T= , LRG_174t1:c.1550+94T= NP_055461.1:n.1550+94T=
XM_005258177.3:c.1661+94T= XP_005258234.1:n.1661+94T=
XM_005258178.2:c.1550+94T= XP_005258235.1:n.1550+94T=
XM_005258179.3:c.1550+94T= XP_005258236.1:n.1550+94T=
XR_935074.1:n.1679+94T=
XM_005258177.4:c.1661+94T= XP_005258234.1:n.1661+94T=
XM_005258178.3:c.1550+94T= XP_005258235.1:n.1550+94T=
XM_005258179.5:c.1550+94T= XP_005258236.1:n.1550+94T=
XM_017026098.1:c.1550+94T= XP_016881587.1:n.1550+94T=
XM_017026099.1:c.1550+94T= XP_016881588.1:n.1550+94T=
XR_935074.2:n.1724+94T=
NM_001375808.1:c.1550+94T= NP_001362737.1:n.1550+94T=
NM_001375809.1:c.1550+94T= NP_001362738.1:n.1550+94T=
NM_001375808.2:c.1550+94T= MANE Select NP_001362737.1:n.1550+94T=