Canonical Allele Identifier: CA201629660

Gene: AGPAT2

Linked Data

• dbSNP Id: rs376021053
• gnomAD v2: 9-139571350-GC-G
• gnomAD v3: 9-136676898-GC-G
• gnomAD v4: 9-136676898-GC-G
• MyVariant Identifiers: chr9:g.139571351del (hg19) ; chr9:g.136676899del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676902del , CM000671.2:g.136676902del	GRCh38
NC_000009.11:g.139571354del , CM000671.1:g.139571354del	GRCh37
NC_000009.10:g.138691175del	NCBI36
NG_008090.1:g.15561del

Transcript Alleles

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