Canonical Allele Identifier: CA5342886

Gene: AGPAT2

Linked Data

• dbSNP Id: rs770435239
• ExAC: 9:139569176 T / TGTGGGG
• gnomAD v2: 9-139569176-T-TGTGGGG
• gnomAD v3: 9-136674724-T-TGTGGGG
• gnomAD v4: 9-136674724-T-TGTGGGG
• MyVariant Identifiers: chr9:g.139569176_139569177insGTGGGG (hg19) ; chr9:g.136674724_136674725insGTGGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674727_136674732dup , CM000671.2:g.136674727_136674732dup	GRCh38
NC_000009.11:g.139569179_139569184dup , CM000671.1:g.139569179_139569184dup	GRCh37
NC_000009.10:g.138689000_138689005dup	NCBI36
NG_008090.1:g.17730_17735dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.661+5_661+10dup MANE Select	ENSP00000360761.2:n.661+5_661+10dup
ENST00000371694.7:c.565+5_565+10dup	ENSP00000360759.3:n.565+5_565+10dup
ENST00000371696.6:c.661+5_661+10dup	ENSP00000360761.2:n.661+5_661+10dup
ENST00000472820.1:n.589+5_589+10dup
ENST00000538402.1:c.661+5_661+10dup	ENSP00000438919.1:n.661+5_661+10dup
NM_001012727.1:c.565+5_565+10dup	NP_001012745.1:n.565+5_565+10dup
NM_006412.3:c.661+5_661+10dup	NP_006403.2:n.661+5_661+10dup
NM_006412.4:c.661+5_661+10dup MANE Select	NP_006403.2:n.661+5_661+10dup
NM_001012727.2:c.565+5_565+10dup	NP_001012745.1:n.565+5_565+10dup