Canonical Allele Identifier: CA2692654841

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676929-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676929_136676930insCA , CM000671.2:g.136676929_136676930insCA	GRCh38
NC_000009.11:g.139571381_139571382insCA , CM000671.1:g.139571381_139571382insCA	GRCh37
NC_000009.10:g.138691202_138691203insCA	NCBI36
NG_008090.1:g.15530_15531insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+31_492+32insTG MANE Select	ENSP00000360761.2:n.492+31_492+32insTG
ENST00000371694.7:c.492+31_492+32insTG	ENSP00000360759.3:n.492+31_492+32insTG
ENST00000371696.6:c.492+31_492+32insTG	ENSP00000360761.2:n.492+31_492+32insTG
ENST00000472820.1:n.420+31_420+32insTG
ENST00000538402.1:c.492+31_492+32insTG	ENSP00000438919.1:n.492+31_492+32insTG
NM_001012727.1:c.492+31_492+32insTG	NP_001012745.1:n.492+31_492+32insTG
NM_006412.3:c.492+31_492+32insTG	NP_006403.2:n.492+31_492+32insTG
NM_006412.4:c.492+31_492+32insTG MANE Select	NP_006403.2:n.492+31_492+32insTG
NM_001012727.2:c.492+31_492+32insTG	NP_001012745.1:n.492+31_492+32insTG