Canonical Allele Identifier: CA2692654115

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674659-A-ATGAGGGGCCCGGGGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674659_136674660insTGAGGGGCCCGGGGCT , CM000671.2:g.136674659_136674660insTGAGGGGCCCGGGGCT	GRCh38
NC_000009.11:g.139569111_139569112insTGAGGGGCCCGGGGCT , CM000671.1:g.139569111_139569112insTGAGGGGCCCGGGGCT	GRCh37
NC_000009.10:g.138688932_138688933insTGAGGGGCCCGGGGCT	NCBI36
NG_008090.1:g.17800_17801insAGCCCCGGGCCCCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.661+75_661+76insAGCCCCGGGCCCCTCA MANE Select	ENSP00000360761.2:n.661+75_661+76insAGCCCCGGGCCCCTCA
ENST00000371694.7:c.565+75_565+76insAGCCCCGGGCCCCTCA	ENSP00000360759.3:n.565+75_565+76insAGCCCCGGGCCCCTCA
ENST00000371696.6:c.661+75_661+76insAGCCCCGGGCCCCTCA	ENSP00000360761.2:n.661+75_661+76insAGCCCCGGGCCCCTCA
ENST00000472820.1:n.589+75_589+76insAGCCCCGGGCCCCTCA
ENST00000538402.1:c.661+75_661+76insAGCCCCGGGCCCCTCA	ENSP00000438919.1:n.661+75_661+76insAGCCCCGGGCCCCTCA
NM_001012727.1:c.565+75_565+76insAGCCCCGGGCCCCTCA	NP_001012745.1:n.565+75_565+76insAGCCCCGGGCCCCTCA
NM_006412.3:c.661+75_661+76insAGCCCCGGGCCCCTCA	NP_006403.2:n.661+75_661+76insAGCCCCGGGCCCCTCA
NM_006412.4:c.661+75_661+76insAGCCCCGGGCCCCTCA MANE Select	NP_006403.2:n.661+75_661+76insAGCCCCGGGCCCCTCA
NM_001012727.2:c.565+75_565+76insAGCCCCGGGCCCCTCA	NP_001012745.1:n.565+75_565+76insAGCCCCGGGCCCCTCA