Canonical Allele Identifier: CA2692653746

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673755-C-CTGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673756_136673759dup , CM000671.2:g.136673756_136673759dup	GRCh38
NC_000009.11:g.139568208_139568211dup , CM000671.1:g.139568208_139568211dup	GRCh37
NC_000009.10:g.138688029_138688032dup	NCBI36
NG_008090.1:g.18701_18704dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.830_833dup MANE Select	ENSP00000360761.2:p.Gln278HisfsTer?
ENST00000371694.7:c.734_737dup	ENSP00000360759.3:p.Gln246HisfsTer?
ENST00000371696.6:c.830_833dup	ENSP00000360761.2:p.Gln278HisfsTer?
ENST00000472820.1:n.758_761dup
ENST00000538402.1:c.830_833dup	ENSP00000438919.1:p.Gln278HisfsTer?
NM_001012727.1:c.734_737dup	NP_001012745.1:p.Gln246HisfsTer?
NM_006412.3:c.830_833dup	NP_006403.2:p.Gln278HisfsTer?
NM_006412.4:c.830_833dup MANE Select	NP_006403.2:p.Gln278HisfsTer?
NM_001012727.2:c.734_737dup	NP_001012745.1:p.Gln246HisfsTer?