Canonical Allele Identifier: CA591367829

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1250048753
• gnomAD v2: 9-139571366-G-GCCCAGGCCCCA
• gnomAD v3: 9-136676914-G-GCCCAGGCCCCA
• gnomAD v4: 9-136676914-G-GCCCAGGCCCCA
• MyVariant Identifiers: chr9:g.139571366_139571367insCCCAGGCCCCA (hg19) ; chr9:g.136676914_136676915insCCCAGGCCCCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676918_136676928dup , CM000671.2:g.136676918_136676928dup	GRCh38
NC_000009.11:g.139571370_139571380dup , CM000671.1:g.139571370_139571380dup	GRCh37
NC_000009.10:g.138691191_138691201dup	NCBI36
NG_008090.1:g.15535_15545dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+36_492+46dup MANE Select	ENSP00000360761.2:n.492+36_492+46dup
ENST00000371694.7:c.492+36_492+46dup	ENSP00000360759.3:n.492+36_492+46dup
ENST00000371696.6:c.492+36_492+46dup	ENSP00000360761.2:n.492+36_492+46dup
ENST00000472820.1:n.420+36_420+46dup
ENST00000538402.1:c.492+36_492+46dup	ENSP00000438919.1:n.492+36_492+46dup
NM_001012727.1:c.492+36_492+46dup	NP_001012745.1:n.492+36_492+46dup
NM_006412.3:c.492+36_492+46dup	NP_006403.2:n.492+36_492+46dup
NM_006412.4:c.492+36_492+46dup MANE Select	NP_006403.2:n.492+36_492+46dup
NM_001012727.2:c.492+36_492+46dup	NP_001012745.1:n.492+36_492+46dup