Canonical Allele Identifier: CA861082084

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1260171069
• gnomAD v3: 9-136676106-AG-A
• gnomAD v4: 9-136676106-AG-A
• MyVariant Identifiers: chr9:g.139570559del (hg19) ; chr9:g.136676107del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676108del , CM000671.2:g.136676108del	GRCh38
NC_000009.11:g.139570560del , CM000671.1:g.139570560del	GRCh37
NC_000009.10:g.138690381del	NCBI36
NG_008090.1:g.16353del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.588+478del MANE Select	ENSP00000360761.2:n.588+478del
ENST00000371694.7:c.492+854del	ENSP00000360759.3:n.492+854del
ENST00000371696.6:c.588+478del	ENSP00000360761.2:n.588+478del
ENST00000472820.1:n.516+478del
ENST00000538402.1:c.588+478del	ENSP00000438919.1:n.588+478del
NM_001012727.1:c.492+854del	NP_001012745.1:n.492+854del
NM_006412.3:c.588+478del	NP_006403.2:n.588+478del
NM_006412.4:c.588+478del MANE Select	NP_006403.2:n.588+478del
NM_001012727.2:c.492+854del	NP_001012745.1:n.492+854del