Canonical Allele Identifier: CA2786278249

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676865_136676866del , CM000671.2:g.136676865_136676866del	GRCh38
NC_000009.11:g.139571317_139571318del , CM000671.1:g.139571317_139571318del	GRCh37
NC_000009.10:g.138691138_138691139del	NCBI36
NG_008090.1:g.15594_15595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+95_492+96del MANE Select	ENSP00000360761.2:n.492+95_492+96del
ENST00000371694.7:c.492+95_492+96del	ENSP00000360759.3:n.492+95_492+96del
ENST00000371696.6:c.492+95_492+96del	ENSP00000360761.2:n.492+95_492+96del
ENST00000472820.1:n.420+95_420+96del
ENST00000538402.1:c.492+95_492+96del	ENSP00000438919.1:n.492+95_492+96del
NM_001012727.1:c.492+95_492+96del	NP_001012745.1:n.492+95_492+96del
NM_006412.3:c.492+95_492+96del	NP_006403.2:n.492+95_492+96del
NM_006412.4:c.492+95_492+96del MANE Select	NP_006403.2:n.492+95_492+96del
NM_001012727.2:c.492+95_492+96del	NP_001012745.1:n.492+95_492+96del