Canonical Allele Identifier: CA2692654093

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674646-C-CCCGGAAATGGGAACGATGAGGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674667_136674668insAGCCGGAAATGGGAACGATGAGG , CM000671.2:g.136674667_136674668insAGCCGGAAATGGGAACGATGAGG	GRCh38
NC_000009.11:g.139569119_139569120insAGCCGGAAATGGGAACGATGAGG , CM000671.1:g.139569119_139569120insAGCCGGAAATGGGAACGATGAGG	GRCh37
NC_000009.10:g.138688940_138688941insAGCCGGAAATGGGAACGATGAGG	NCBI36
NG_008090.1:g.17813_17814insCTCCTCATCGTTCCCATTTCCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG MANE Select	ENSP00000360761.2:n.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG
ENST00000371694.7:c.565+88_565+89insCTCCTCATCGTTCCCATTTCCGG	ENSP00000360759.3:n.565+88_565+89insCTCCTCATCGTTCCCATTTCCGG
ENST00000371696.6:c.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG	ENSP00000360761.2:n.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG
ENST00000472820.1:n.589+88_589+89insCTCCTCATCGTTCCCATTTCCGG
ENST00000538402.1:c.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG	ENSP00000438919.1:n.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG
NM_001012727.1:c.565+88_565+89insCTCCTCATCGTTCCCATTTCCGG	NP_001012745.1:n.565+88_565+89insCTCCTCATCGTTCCCATTTCCGG
NM_006412.3:c.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG	NP_006403.2:n.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG
NM_006412.4:c.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG MANE Select	NP_006403.2:n.661+88_661+89insCTCCTCATCGTTCCCATTTCCGG
NM_001012727.2:c.565+88_565+89insCTCCTCATCGTTCCCATTTCCGG	NP_001012745.1:n.565+88_565+89insCTCCTCATCGTTCCCATTTCCGG