Canonical Allele Identifier: CA2692654791

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676909-G-GGCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676909_136676910insGCCCCCCCC , CM000671.2:g.136676909_136676910insGCCCCCCCC	GRCh38
NC_000009.11:g.139571361_139571362insGCCCCCCCC , CM000671.1:g.139571361_139571362insGCCCCCCCC	GRCh37
NC_000009.10:g.138691182_138691183insGCCCCCCCC	NCBI36
NG_008090.1:g.15550_15551insGGGGGGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+51_492+52insGGGGGGGGC MANE Select	ENSP00000360761.2:n.492+51_492+52insGGGGGGGGC
ENST00000371694.7:c.492+51_492+52insGGGGGGGGC	ENSP00000360759.3:n.492+51_492+52insGGGGGGGGC
ENST00000371696.6:c.492+51_492+52insGGGGGGGGC	ENSP00000360761.2:n.492+51_492+52insGGGGGGGGC
ENST00000472820.1:n.420+51_420+52insGGGGGGGGC
ENST00000538402.1:c.492+51_492+52insGGGGGGGGC	ENSP00000438919.1:n.492+51_492+52insGGGGGGGGC
NM_001012727.1:c.492+51_492+52insGGGGGGGGC	NP_001012745.1:n.492+51_492+52insGGGGGGGGC
NM_006412.3:c.492+51_492+52insGGGGGGGGC	NP_006403.2:n.492+51_492+52insGGGGGGGGC
NM_006412.4:c.492+51_492+52insGGGGGGGGC MANE Select	NP_006403.2:n.492+51_492+52insGGGGGGGGC
NM_001012727.2:c.492+51_492+52insGGGGGGGGC	NP_001012745.1:n.492+51_492+52insGGGGGGGGC