Canonical Allele Identifier: CA591367772

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1378768676
• gnomAD v2: 9-139568383-T-TG
• gnomAD v4: 9-136673931-T-TG
• MyVariant Identifiers: chr9:g.139568383_139568384insG (hg19) ; chr9:g.136673931_136673932insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673936dup , CM000671.2:g.136673936dup	GRCh38
NC_000009.11:g.139568388dup , CM000671.1:g.139568388dup	GRCh37
NC_000009.10:g.138688209dup	NCBI36
NG_008090.1:g.18528dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.662-5dup MANE Select	ENSP00000360761.2:n.662-5dup
ENST00000371694.7:c.566-5dup	ENSP00000360759.3:n.566-5dup
ENST00000371696.6:c.662-5dup	ENSP00000360761.2:n.662-5dup
ENST00000472820.1:n.590-5dup
ENST00000538402.1:c.662-5dup	ENSP00000438919.1:n.662-5dup
NM_001012727.1:c.566-5dup	NP_001012745.1:n.566-5dup
NM_006412.3:c.662-5dup	NP_006403.2:n.662-5dup
NM_006412.4:c.662-5dup MANE Select	NP_006403.2:n.662-5dup
NM_001012727.2:c.566-5dup	NP_001012745.1:n.566-5dup