Canonical Allele Identifier: CA2579519986

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676739_136676743dup , CM000671.2:g.136676739_136676743dup	GRCh38
NC_000009.11:g.139571191_139571195dup , CM000671.1:g.139571191_139571195dup	GRCh37
NC_000009.10:g.138691012_138691016dup	NCBI36
NG_008090.1:g.15718_15722dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.493-62_493-58dup MANE Select	ENSP00000360761.2:n.493-62_493-58dup
ENST00000371694.7:c.492+219_492+223dup	ENSP00000360759.3:n.492+219_492+223dup
ENST00000371696.6:c.493-62_493-58dup	ENSP00000360761.2:n.493-62_493-58dup
ENST00000472820.1:n.421-62_421-58dup
ENST00000538402.1:c.493-62_493-58dup	ENSP00000438919.1:n.493-62_493-58dup
NM_001012727.1:c.492+219_492+223dup	NP_001012745.1:n.492+219_492+223dup
NM_006412.3:c.493-62_493-58dup	NP_006403.2:n.493-62_493-58dup
NM_006412.4:c.493-62_493-58dup MANE Select	NP_006403.2:n.493-62_493-58dup
NM_001012727.2:c.492+219_492+223dup	NP_001012745.1:n.492+219_492+223dup