Canonical Allele Identifier: CA2223746811

Gene: LPCAT2 CAPNS2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55566939_55566940delinsTC , CM000678.2:g.55566939_55566940delinsTC	GRCh38
NC_000016.9:g.55600851_55600852delinsTC , CM000678.1:g.55600851_55600852delinsTC	GRCh37
NC_000016.8:g.54158352_54158353delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262134.10:c.1216-7692_1216-7691delinsTC (LPCAT2) MANE Select	ENSP00000262134.5:n.1216-7692_1216-7691delinsTC
ENST00000457326.3:c.183_184delinsTC (CAPNS2) MANE Select	ENSP00000400882.2:p.Pro61=
ENST00000262134.9:c.1216-7692_1216-7691delinsTC (LPCAT2)	ENSP00000262134.5:n.1216-7692_1216-7691delinsTC
ENST00000457326.2:c.183_184delinsTC (CAPNS2)	ENSP00000400882.2:p.Pro61=
ENST00000563095.5:n.614-7692_614-7691delinsTC (LPCAT2)
ENST00000565056.1:n.90-7692_90-7691delinsTC (LPCAT2)
ENST00000566915.5:n.1298-7692_1298-7691delinsTC (LPCAT2)
ENST00000615823.1:c.340-7692_340-7691delinsTC (LPCAT2)	ENSP00000483225.1:n.340-7692_340-7691delinsTC
NM_017839.4:c.1216-7692_1216-7691delinsTC (LPCAT2)	NP_060309.2:n.1216-7692_1216-7691delinsTC
NM_032330.1:c.183_184delinsTC (CAPNS2)	NP_115706.1:p.Pro61=
XM_006721211.2:c.1048-7692_1048-7691delinsTC (LPCAT2)	XP_006721274.1:n.1048-7692_1048-7691delinsTC
XM_011523169.1:c.406-7692_406-7691delinsTC (LPCAT2)	XP_011521471.1:n.406-7692_406-7691delinsTC
NM_032330.2:c.183_184delinsTC (CAPNS2)	NP_115706.1:p.Pro61=
XM_011523169.3:c.406-7692_406-7691delinsTC (LPCAT2)	XP_011521471.1:n.406-7692_406-7691delinsTC
XM_017023376.1:c.1048-7692_1048-7691delinsTC (LPCAT2)	XP_016878865.1:n.1048-7692_1048-7691delinsTC
NM_017839.5:c.1216-7692_1216-7691delinsTC (LPCAT2) MANE Select	NP_060309.2:n.1216-7692_1216-7691delinsTC
NM_032330.3:c.183_184delinsTC (CAPNS2) MANE Select	NP_115706.1:p.Pro61=