Canonical Allele Identifier: CA2692654776

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676906-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676906_136676907insA , CM000671.2:g.136676906_136676907insA	GRCh38
NC_000009.11:g.139571358_139571359insA , CM000671.1:g.139571358_139571359insA	GRCh37
NC_000009.10:g.138691179_138691180insA	NCBI36
NG_008090.1:g.15553_15554insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+54_492+55insT MANE Select	ENSP00000360761.2:n.492+54_492+55insT
ENST00000371694.7:c.492+54_492+55insT	ENSP00000360759.3:n.492+54_492+55insT
ENST00000371696.6:c.492+54_492+55insT	ENSP00000360761.2:n.492+54_492+55insT
ENST00000472820.1:n.420+54_420+55insT
ENST00000538402.1:c.492+54_492+55insT	ENSP00000438919.1:n.492+54_492+55insT
NM_001012727.1:c.492+54_492+55insT	NP_001012745.1:n.492+54_492+55insT
NM_006412.3:c.492+54_492+55insT	NP_006403.2:n.492+54_492+55insT
NM_006412.4:c.492+54_492+55insT MANE Select	NP_006403.2:n.492+54_492+55insT
NM_001012727.2:c.492+54_492+55insT	NP_001012745.1:n.492+54_492+55insT