Canonical Allele Identifier: CA2692653765

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673865-G-GGACGTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673867_136673873dup , CM000671.2:g.136673867_136673873dup	GRCh38
NC_000009.11:g.139568319_139568325dup , CM000671.1:g.139568319_139568325dup	GRCh37
NC_000009.10:g.138688140_138688146dup	NCBI36
NG_008090.1:g.18588_18594dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.717_723dup MANE Select	ENSP00000360761.2:p.Pro242GlyfsTer?
ENST00000371694.7:c.621_627dup	ENSP00000360759.3:p.Pro210GlyfsTer?
ENST00000371696.6:c.717_723dup	ENSP00000360761.2:p.Pro242GlyfsTer?
ENST00000472820.1:n.645_651dup
ENST00000538402.1:c.717_723dup	ENSP00000438919.1:p.Pro242GlyfsTer?
NM_001012727.1:c.621_627dup	NP_001012745.1:p.Pro210GlyfsTer?
NM_006412.3:c.717_723dup	NP_006403.2:p.Pro242GlyfsTer?
NM_006412.4:c.717_723dup MANE Select	NP_006403.2:p.Pro242GlyfsTer?
NM_001012727.2:c.621_627dup	NP_001012745.1:p.Pro210GlyfsTer?