Canonical Allele Identifier: CA1130022093

Gene: AGPAT2

Linked Data

• gnomAD v3: 9-136687304-C-CTTAAAA
• gnomAD v4: 9-136687304-C-CTTAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687304_136687305insTTAAAA , CM000671.2:g.136687304_136687305insTTAAAA	GRCh38
NC_000009.11:g.139581756_139581757insTTAAAA , CM000671.1:g.139581756_139581757insTTAAAA	GRCh37
NC_000009.10:g.138701577_138701578insTTAAAA	NCBI36
NG_008090.1:g.5155_5156insTTTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.53_54insTTTTAA MANE Select	ENSP00000360761.2:p.Val18_Gln19insPheLys
ENST00000371694.7:c.53_54insTTTTAA	ENSP00000360759.3:p.Val18_Gln19insPheLys
ENST00000371696.6:c.53_54insTTTTAA	ENSP00000360761.2:p.Val18_Gln19insPheLys
ENST00000470861.1:n.61_62insTTTTAA
ENST00000538402.1:c.53_54insTTTTAA	ENSP00000438919.1:p.Val18_Gln19insPheLys
NM_001012727.1:c.53_54insTTTTAA	NP_001012745.1:p.Val18_Gln19insPheLys
NM_006412.3:c.53_54insTTTTAA	NP_006403.2:p.Val18_Gln19insPheLys
NM_006412.4:c.53_54insTTTTAA MANE Select	NP_006403.2:p.Val18_Gln19insPheLys
NM_001012727.2:c.53_54insTTTTAA	NP_001012745.1:p.Val18_Gln19insPheLys