Canonical Allele Identifier: CA2579519913

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674693_136674696dup , CM000671.2:g.136674693_136674696dup	GRCh38
NC_000009.11:g.139569145_139569148dup , CM000671.1:g.139569145_139569148dup	GRCh37
NC_000009.10:g.138688966_138688969dup	NCBI36
NG_008090.1:g.17765_17768dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.661+40_661+43dup MANE Select	ENSP00000360761.2:n.661+40_661+43dup
ENST00000371694.7:c.565+40_565+43dup	ENSP00000360759.3:n.565+40_565+43dup
ENST00000371696.6:c.661+40_661+43dup	ENSP00000360761.2:n.661+40_661+43dup
ENST00000472820.1:n.589+40_589+43dup
ENST00000538402.1:c.661+40_661+43dup	ENSP00000438919.1:n.661+40_661+43dup
NM_001012727.1:c.565+40_565+43dup	NP_001012745.1:n.565+40_565+43dup
NM_006412.3:c.661+40_661+43dup	NP_006403.2:n.661+40_661+43dup
NM_006412.4:c.661+40_661+43dup MANE Select	NP_006403.2:n.661+40_661+43dup
NM_001012727.2:c.565+40_565+43dup	NP_001012745.1:n.565+40_565+43dup