Canonical Allele Identifier: CA2557216384

Gene: LPCAT2 CAPNS2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55566910_55566911insT , CM000678.2:g.55566910_55566911insT	GRCh38
NC_000016.9:g.55600822_55600823insT , CM000678.1:g.55600822_55600823insT	GRCh37
NC_000016.8:g.54158323_54158324insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262134.10:c.1216-7721_1216-7720insT (LPCAT2) MANE Select	ENSP00000262134.5:n.1216-7721_1216-7720insT
ENST00000457326.3:c.154_155insT (CAPNS2) MANE Select	ENSP00000400882.2:p.Ala52ValfsTer25
ENST00000262134.9:c.1216-7721_1216-7720insT (LPCAT2)	ENSP00000262134.5:n.1216-7721_1216-7720insT
ENST00000457326.2:c.154_155insT (CAPNS2)	ENSP00000400882.2:p.Ala52ValfsTer25
ENST00000563095.5:n.614-7721_614-7720insT (LPCAT2)
ENST00000565056.1:n.90-7721_90-7720insT (LPCAT2)
ENST00000566915.5:n.1298-7721_1298-7720insT (LPCAT2)
ENST00000615823.1:c.340-7721_340-7720insT (LPCAT2)	ENSP00000483225.1:n.340-7721_340-7720insT
NM_017839.4:c.1216-7721_1216-7720insT (LPCAT2)	NP_060309.2:n.1216-7721_1216-7720insT
NM_032330.1:c.154_155insT (CAPNS2)	NP_115706.1:p.Ala52ValfsTer25
XM_006721211.2:c.1048-7721_1048-7720insT (LPCAT2)	XP_006721274.1:n.1048-7721_1048-7720insT
XM_011523169.1:c.406-7721_406-7720insT (LPCAT2)	XP_011521471.1:n.406-7721_406-7720insT
NM_032330.2:c.154_155insT (CAPNS2)	NP_115706.1:p.Ala52ValfsTer25
XM_011523169.3:c.406-7721_406-7720insT (LPCAT2)	XP_011521471.1:n.406-7721_406-7720insT
XM_017023376.1:c.1048-7721_1048-7720insT (LPCAT2)	XP_016878865.1:n.1048-7721_1048-7720insT
NM_017839.5:c.1216-7721_1216-7720insT (LPCAT2) MANE Select	NP_060309.2:n.1216-7721_1216-7720insT
NM_032330.3:c.154_155insT (CAPNS2) MANE Select	NP_115706.1:p.Ala52ValfsTer25