Canonical Allele Identifier: CA2692654766

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676899-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676899_136676900insA , CM000671.2:g.136676899_136676900insA	GRCh38
NC_000009.11:g.139571351_139571352insA , CM000671.1:g.139571351_139571352insA	GRCh37
NC_000009.10:g.138691172_138691173insA	NCBI36
NG_008090.1:g.15560_15561insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+61_492+62insT MANE Select	ENSP00000360761.2:n.492+61_492+62insT
ENST00000371694.7:c.492+61_492+62insT	ENSP00000360759.3:n.492+61_492+62insT
ENST00000371696.6:c.492+61_492+62insT	ENSP00000360761.2:n.492+61_492+62insT
ENST00000472820.1:n.420+61_420+62insT
ENST00000538402.1:c.492+61_492+62insT	ENSP00000438919.1:n.492+61_492+62insT
NM_001012727.1:c.492+61_492+62insT	NP_001012745.1:n.492+61_492+62insT
NM_006412.3:c.492+61_492+62insT	NP_006403.2:n.492+61_492+62insT
NM_006412.4:c.492+61_492+62insT MANE Select	NP_006403.2:n.492+61_492+62insT
NM_001012727.2:c.492+61_492+62insT	NP_001012745.1:n.492+61_492+62insT