Canonical Allele Identifier: CA861082707

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1240386767
• gnomAD v4: 9-136676839-TGC-T
• MyVariant Identifiers: chr9:g.139571292_139571293del (hg19) ; chr9:g.136676840_136676841del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676841_136676842del , CM000671.2:g.136676841_136676842del	GRCh38
NC_000009.11:g.139571293_139571294del , CM000671.1:g.139571293_139571294del	GRCh37
NC_000009.10:g.138691114_138691115del	NCBI36
NG_008090.1:g.15619_15620del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+120_492+121del MANE Select	ENSP00000360761.2:n.492+120_492+121del
ENST00000371694.7:c.492+120_492+121del	ENSP00000360759.3:n.492+120_492+121del
ENST00000371696.6:c.492+120_492+121del	ENSP00000360761.2:n.492+120_492+121del
ENST00000472820.1:n.420+120_420+121del
ENST00000538402.1:c.492+120_492+121del	ENSP00000438919.1:n.492+120_492+121del
NM_001012727.1:c.492+120_492+121del	NP_001012745.1:n.492+120_492+121del
NM_006412.3:c.492+120_492+121del	NP_006403.2:n.492+120_492+121del
NM_006412.4:c.492+120_492+121del MANE Select	NP_006403.2:n.492+120_492+121del
NM_001012727.2:c.492+120_492+121del	NP_001012745.1:n.492+120_492+121del