Canonical Allele Identifier: CA2692654814

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676917-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676918_136676919del , CM000671.2:g.136676918_136676919del	GRCh38
NC_000009.11:g.139571370_139571371del , CM000671.1:g.139571370_139571371del	GRCh37
NC_000009.10:g.138691191_138691192del	NCBI36
NG_008090.1:g.15541_15542del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+42_492+43del MANE Select	ENSP00000360761.2:n.492+42_492+43del
ENST00000371694.7:c.492+42_492+43del	ENSP00000360759.3:n.492+42_492+43del
ENST00000371696.6:c.492+42_492+43del	ENSP00000360761.2:n.492+42_492+43del
ENST00000472820.1:n.420+42_420+43del
ENST00000538402.1:c.492+42_492+43del	ENSP00000438919.1:n.492+42_492+43del
NM_001012727.1:c.492+42_492+43del	NP_001012745.1:n.492+42_492+43del
NM_006412.3:c.492+42_492+43del	NP_006403.2:n.492+42_492+43del
NM_006412.4:c.492+42_492+43del MANE Select	NP_006403.2:n.492+42_492+43del
NM_001012727.2:c.492+42_492+43del	NP_001012745.1:n.492+42_492+43del