Canonical Allele Identifier: CA502690424

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2960742G>T , CM000680.2:g.2960742G>T	GRCh38
NC_000018.9:g.2960740G>T , CM000680.1:g.2960740G>T	GRCh37
NC_000018.8:g.2950740G>T	NCBI36
NG_007507.1:g.56206C>A , LRG_174:g.56206C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001375808.2:c.99C>A MANE Select	NP_001362737.1:p.Val33=
ENST00000677752.1:c.99C>A MANE Select	ENSP00000504857.1:p.Val33=
NM_001375808.1:c.99C>A	NP_001362737.1:p.Val33=
NM_001375809.1:c.99C>A	NP_001362738.1:p.Val33=
NM_014646.2:c.99C>A , LRG_174t1:c.99C>A	NP_055461.1:p.Val33=
ENST00000261596.8:c.99C>A	ENSP00000261596.4:p.Val33=
ENST00000261596.9:c.99C>A	ENSP00000261596.4:p.Val33=
ENST00000584294.1:c.99C>A	ENSP00000463026.1:p.Val33=
ENST00000584915.1:c.210C>A	ENSP00000463810.1:p.Val70=
ENST00000584915.2:c.210C>A	ENSP00000463810.2:p.Val70=
ENST00000697039.1:c.99C>A	ENSP00000513061.1:p.Val33=
ENST00000697040.1:c.99C>A	ENSP00000513062.1:p.Val33=
ENST00000697042.1:c.99C>A	ENSP00000513064.1:p.Val33=
ENST00000697043.1:c.99C>A	ENSP00000513065.1:p.Val33=
XM_005258177.3:c.210C>A	XP_005258234.1:p.Val70=
XM_005258177.4:c.210C>A	XP_005258234.1:p.Val70=
XM_005258178.2:c.99C>A	XP_005258235.1:p.Val33=
XM_005258178.3:c.99C>A	XP_005258235.1:p.Val33=
XM_005258179.3:c.99C>A	XP_005258236.1:p.Val33=
XM_005258179.5:c.99C>A	XP_005258236.1:p.Val33=
XM_017026098.1:c.99C>A	XP_016881587.1:p.Val33=
XM_017026099.1:c.99C>A	XP_016881588.1:p.Val33=
XR_935074.1:n.228C>A
XR_935074.2:n.273C>A