Canonical Allele Identifier: CA2280788044
Gene: LPIN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2922057C= , CM000680.2:g.2922057C= GRCh38
NC_000018.9:g.2922055C= , CM000680.1:g.2922055C= GRCh37
NC_000018.8:g.2912055C= NCBI36
NG_007507.1:g.94891G= , LRG_174:g.94891G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261596.9:c.2317G= ENSP00000261596.4:p.Ala773=
ENST00000697039.1:c.2317G= ENSP00000513061.1:p.Ala773=
ENST00000697040.1:c.2317G= ENSP00000513062.1:p.Ala773=
ENST00000697041.1:c.1012G= ENSP00000513063.1:p.Ala338=
ENST00000677752.1:c.2317G= MANE Select ENSP00000504857.1:p.Ala773=
ENST00000261596.8:c.2317G= ENSP00000261596.4:p.Ala773=
NM_014646.2:c.2317G= , LRG_174t1:c.2317G= NP_055461.1:p.Ala773=
XM_005258177.3:c.2428G= XP_005258234.1:p.Ala810=
XM_005258178.2:c.2317G= XP_005258235.1:p.Ala773=
XM_005258179.3:c.2317G= XP_005258236.1:p.Ala773=
XM_005258177.4:c.2428G= XP_005258234.1:p.Ala810=
XM_005258178.3:c.2317G= XP_005258235.1:p.Ala773=
XM_005258179.5:c.2317G= XP_005258236.1:p.Ala773=
XM_017026098.1:c.2317G= XP_016881587.1:p.Ala773=
XM_017026099.1:c.2317G= XP_016881588.1:p.Ala773=
NM_001375808.1:c.2317G= NP_001362737.1:p.Ala773=
NM_001375809.1:c.2317G= NP_001362738.1:p.Ala773=
NM_001375808.2:c.2317G= MANE Select NP_001362737.1:p.Ala773=