Canonical Allele Identifier: CA2223746906

Gene: LPCAT2 CAPNS2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55567040_55567041delinsTG , CM000678.2:g.55567040_55567041delinsTG	GRCh38
NC_000016.9:g.55600952_55600953delinsTG , CM000678.1:g.55600952_55600953delinsTG	GRCh37
NC_000016.8:g.54158453_54158454delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262134.10:c.1216-7591_1216-7590delinsTG (LPCAT2) MANE Select	ENSP00000262134.5:n.1216-7591_1216-7590delinsTG
ENST00000457326.3:c.284_285delinsTG (CAPNS2) MANE Select	ENSP00000400882.2:p.Val95=
ENST00000262134.9:c.1216-7591_1216-7590delinsTG (LPCAT2)	ENSP00000262134.5:n.1216-7591_1216-7590delinsTG
ENST00000457326.2:c.284_285delinsTG (CAPNS2)	ENSP00000400882.2:p.Val95=
ENST00000563095.5:n.614-7591_614-7590delinsTG (LPCAT2)
ENST00000565056.1:n.90-7591_90-7590delinsTG (LPCAT2)
ENST00000566915.5:n.1298-7591_1298-7590delinsTG (LPCAT2)
ENST00000615823.1:c.340-7591_340-7590delinsTG (LPCAT2)	ENSP00000483225.1:n.340-7591_340-7590delinsTG
NM_017839.4:c.1216-7591_1216-7590delinsTG (LPCAT2)	NP_060309.2:n.1216-7591_1216-7590delinsTG
NM_032330.1:c.284_285delinsTG (CAPNS2)	NP_115706.1:p.Val95=
XM_006721211.2:c.1048-7591_1048-7590delinsTG (LPCAT2)	XP_006721274.1:n.1048-7591_1048-7590delinsTG
XM_011523169.1:c.406-7591_406-7590delinsTG (LPCAT2)	XP_011521471.1:n.406-7591_406-7590delinsTG
NM_032330.2:c.284_285delinsTG (CAPNS2)	NP_115706.1:p.Val95=
XM_011523169.3:c.406-7591_406-7590delinsTG (LPCAT2)	XP_011521471.1:n.406-7591_406-7590delinsTG
XM_017023376.1:c.1048-7591_1048-7590delinsTG (LPCAT2)	XP_016878865.1:n.1048-7591_1048-7590delinsTG
NM_017839.5:c.1216-7591_1216-7590delinsTG (LPCAT2) MANE Select	NP_060309.2:n.1216-7591_1216-7590delinsTG
NM_032330.3:c.284_285delinsTG (CAPNS2) MANE Select	NP_115706.1:p.Val95=