Canonical Allele Identifier: CA591367863

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1320364369
• gnomAD v2: 9-139581571-G-GGGAAGC
• gnomAD v3: 9-136687119-G-GGGAAGC
• gnomAD v4: 9-136687119-G-GGGAAGC
• MyVariant Identifiers: chr9:g.139581571_139581572insGGAAGC (hg19) ; chr9:g.136687119_136687120insGGAAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687128_136687133dup , CM000671.2:g.136687128_136687133dup	GRCh38
NC_000009.11:g.139581580_139581585dup , CM000671.1:g.139581580_139581585dup	GRCh37
NC_000009.10:g.138701401_138701406dup	NCBI36
NG_008090.1:g.5335_5340dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+51_182+56dup MANE Select	ENSP00000360761.2:n.182+51_182+56dup
ENST00000371694.7:c.182+51_182+56dup	ENSP00000360759.3:n.182+51_182+56dup
ENST00000371696.6:c.182+51_182+56dup	ENSP00000360761.2:n.182+51_182+56dup
ENST00000470861.1:n.190+51_190+56dup
ENST00000538402.1:c.182+51_182+56dup	ENSP00000438919.1:n.182+51_182+56dup
NM_001012727.1:c.182+51_182+56dup	NP_001012745.1:n.182+51_182+56dup
NM_006412.3:c.182+51_182+56dup	NP_006403.2:n.182+51_182+56dup
NM_006412.4:c.182+51_182+56dup MANE Select	NP_006403.2:n.182+51_182+56dup
NM_001012727.2:c.182+51_182+56dup	NP_001012745.1:n.182+51_182+56dup