Canonical Allele Identifier: CA1130033669

Gene: AGPAT2

Linked Data

• gnomAD v3: 9-136674636-A-ACGGGTGCCACCCGGAAATGGGAACGATGAGGGGCCCGGGGCTCCGTGACTGTAGGGTCAGGCGGGGCCTACACCC
• gnomAD v4: 9-136674636-A-ACGGGTGCCACCCGGAAATGGGAACGATGAGGGGCCCGGGGCTCCGTGACTGTAGGGTCAGGCGGGGCCTACACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674644_136674718dup , CM000671.2:g.136674644_136674718dup	GRCh38
NC_000009.11:g.139569096_139569170dup , CM000671.1:g.139569096_139569170dup	GRCh37
NC_000009.10:g.138688917_138688991dup	NCBI36
NG_008090.1:g.17749_17823dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.661+24_661+98dup MANE Select	ENSP00000360761.2:n.661+24_661+98dup
ENST00000371694.7:c.565+24_565+98dup	ENSP00000360759.3:n.565+24_565+98dup
ENST00000371696.6:c.661+24_661+98dup	ENSP00000360761.2:n.661+24_661+98dup
ENST00000472820.1:n.589+24_589+98dup
ENST00000538402.1:c.661+24_661+98dup	ENSP00000438919.1:n.661+24_661+98dup
NM_001012727.1:c.565+24_565+98dup	NP_001012745.1:n.565+24_565+98dup
NM_006412.3:c.661+24_661+98dup	NP_006403.2:n.661+24_661+98dup
NM_006412.4:c.661+24_661+98dup MANE Select	NP_006403.2:n.661+24_661+98dup
NM_001012727.2:c.565+24_565+98dup	NP_001012745.1:n.565+24_565+98dup