Canonical Allele Identifier: CA201629648

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1016313266
• gnomAD v3: 9-136676854-ATGTGGGGGTCT-A
• gnomAD v4: 9-136676854-ATGTGGGGGTCT-A
• MyVariant Identifiers: chr9:g.139571307_139571317del (hg19) ; chr9:g.136676855_136676865del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676858_136676868del , CM000671.2:g.136676858_136676868del	GRCh38
NC_000009.11:g.139571310_139571320del , CM000671.1:g.139571310_139571320del	GRCh37
NC_000009.10:g.138691131_138691141del	NCBI36
NG_008090.1:g.15595_15605del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+96_492+106del MANE Select	ENSP00000360761.2:n.492+96_492+106del
ENST00000371694.7:c.492+96_492+106del	ENSP00000360759.3:n.492+96_492+106del
ENST00000371696.6:c.492+96_492+106del	ENSP00000360761.2:n.492+96_492+106del
ENST00000472820.1:n.420+96_420+106del
ENST00000538402.1:c.492+96_492+106del	ENSP00000438919.1:n.492+96_492+106del
NM_001012727.1:c.492+96_492+106del	NP_001012745.1:n.492+96_492+106del
NM_006412.3:c.492+96_492+106del	NP_006403.2:n.492+96_492+106del
NM_006412.4:c.492+96_492+106del MANE Select	NP_006403.2:n.492+96_492+106del
NM_001012727.2:c.492+96_492+106del	NP_001012745.1:n.492+96_492+106del