Canonical Allele Identifier: CA2280788058

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2922091G= , CM000680.2:g.2922091G=	GRCh38
NC_000018.9:g.2922089G= , CM000680.1:g.2922089G=	GRCh37
NC_000018.8:g.2912089G=	NCBI36
NG_007507.1:g.94857C= , LRG_174:g.94857C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261596.9:c.2283C=	ENSP00000261596.4:p.Gly761=
ENST00000697039.1:c.2283C=	ENSP00000513061.1:p.Gly761=
ENST00000697040.1:c.2283C=	ENSP00000513062.1:p.Gly761=
ENST00000697041.1:c.978C=	ENSP00000513063.1:p.Gly326=
ENST00000677752.1:c.2283C= MANE Select	ENSP00000504857.1:p.Gly761=
ENST00000261596.8:c.2283C=	ENSP00000261596.4:p.Gly761=
NM_014646.2:c.2283C= , LRG_174t1:c.2283C=	NP_055461.1:p.Gly761=
XM_005258177.3:c.2394C=	XP_005258234.1:p.Gly798=
XM_005258178.2:c.2283C=	XP_005258235.1:p.Gly761=
XM_005258179.3:c.2283C=	XP_005258236.1:p.Gly761=
XM_005258177.4:c.2394C=	XP_005258234.1:p.Gly798=
XM_005258178.3:c.2283C=	XP_005258235.1:p.Gly761=
XM_005258179.5:c.2283C=	XP_005258236.1:p.Gly761=
XM_017026098.1:c.2283C=	XP_016881587.1:p.Gly761=
XM_017026099.1:c.2283C=	XP_016881588.1:p.Gly761=
NM_001375808.1:c.2283C=	NP_001362737.1:p.Gly761=
NM_001375809.1:c.2283C=	NP_001362738.1:p.Gly761=
NM_001375808.2:c.2283C= MANE Select	NP_001362737.1:p.Gly761=