Canonical Allele Identifier: CA2280800513

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2948031C= , CM000680.2:g.2948031C=	GRCh38
NC_000018.9:g.2948029C= , CM000680.1:g.2948029C=	GRCh37
NC_000018.8:g.2938029C=	NCBI36
NG_007507.1:g.68917G= , LRG_174:g.68917G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001375808.2:c.590+3024G= MANE Select	NP_001362737.1:n.590+3024G=
ENST00000677752.1:c.590+3024G= MANE Select	ENSP00000504857.1:n.590+3024G=
NM_001375808.1:c.590+3024G=	NP_001362737.1:n.590+3024G=
NM_001375809.1:c.590+3024G=	NP_001362738.1:n.590+3024G=
NM_014646.2:c.590+3024G= , LRG_174t1:c.590+3024G=	NP_055461.1:n.590+3024G=
ENST00000261596.8:c.590+3024G=	ENSP00000261596.4:n.590+3024G=
ENST00000261596.9:c.590+3024G=	ENSP00000261596.4:n.590+3024G=
ENST00000584294.1:c.590+3024G=	ENSP00000463026.1:n.590+3024G=
ENST00000697039.1:c.590+3024G=	ENSP00000513061.1:n.590+3024G=
ENST00000697040.1:c.590+3024G=	ENSP00000513062.1:n.590+3024G=
ENST00000697042.1:c.590+3024G=	ENSP00000513064.1:n.590+3024G=
XM_005258177.3:c.701+3024G=	XP_005258234.1:n.701+3024G=
XM_005258177.4:c.701+3024G=	XP_005258234.1:n.701+3024G=
XM_005258178.2:c.590+3024G=	XP_005258235.1:n.590+3024G=
XM_005258178.3:c.590+3024G=	XP_005258235.1:n.590+3024G=
XM_005258179.3:c.590+3024G=	XP_005258236.1:n.590+3024G=
XM_005258179.5:c.590+3024G=	XP_005258236.1:n.590+3024G=
XM_017026098.1:c.590+3024G=	XP_016881587.1:n.590+3024G=
XM_017026099.1:c.590+3024G=	XP_016881588.1:n.590+3024G=
XR_935074.1:n.719+3024G=
XR_935074.2:n.764+3024G=