Canonical Allele Identifier: CA591186737

Gene: AGPAT2

Linked Data

• gnomAD v2: 9-139581441-G-GTGACTCCGGGACCCCCTGACTCCGGGACCCCGTGACTCCGGGACCCCC
• gnomAD v3: 9-136686989-G-GTGACTCCGGGACCCCCTGACTCCGGGACCCCGTGACTCCGGGACCCCC
• gnomAD v4: 9-136686989-G-GTGACTCCGGGACCCCCTGACTCCGGGACCCCGTGACTCCGGGACCCCC
• MyVariant Identifiers: chr9:g.139581457_139581458insTGACTCCGGGACCCCGTGACTCCGGGACCCCCTGACTCCGGGACCCCC (hg19) ; chr9:g.136687005_136687006insTGACTCCGGGACCCCGTGACTCCGGGACCCCCTGACTCCGGGACCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687020_136687021insGTGACTCCGGGACCCCCTGACTCCGGGACCCCCTGACTCCGGGACCCC , CM000671.2:g.136687020_136687021insGTGACTCCGGGACCCCCTGACTCCGGGACCCCCTGACTCCGGGACCCC	GRCh38
NC_000009.11:g.139581472_139581473insGTGACTCCGGGACCCCCTGACTCCGGGACCCCCTGACTCCGGGACCCC , CM000671.1:g.139581472_139581473insGTGACTCCGGGACCCCCTGACTCCGGGACCCCCTGACTCCGGGACCCC	GRCh37
NC_000009.10:g.138701293_138701294insGTGACTCCGGGACCCCCTGACTCCGGGACCCCCTGACTCCGGGACCCC	NCBI36
NG_008090.1:g.5470_5471insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA MANE Select	ENSP00000360761.2:n.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTC...
ENST00000371694.7:c.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA	ENSP00000360759.3:n.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTC...
ENST00000371696.6:c.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA	ENSP00000360761.2:n.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTC...
ENST00000470861.1:n.190+186_190+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA
ENST00000538402.1:c.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA	ENSP00000438919.1:n.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTC...
NM_001012727.1:c.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA	NP_001012745.1:n.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCG...
NM_006412.3:c.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA	NP_006403.2:n.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAG...
NM_006412.4:c.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA MANE Select	NP_006403.2:n.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAG...
NM_001012727.2:c.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCGGAGTCAGGGGGTCCCGGAGTCA	NP_001012745.1:n.182+186_182+187insGGGGGTCCCGGAGTCACGGGGTCCCG...