Canonical Allele Identifier: CA2692654447

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674946-C-CTGCCTGGGCACCAGGTGCCCACGTTCTGGGAACTGGCTGGAAGGGGCAAGAGGTCATGAGCCCCGCAGCCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674950_136674951insTGGGCACCAGGTGCCCACGTTCTGGGAACTGGCTGGAAGGGGCAAGAGGTCATGAGCCCCGCAGCCTGTGCC , CM000671.2:g.136674950_136674951insTGGGCACCAGGTGCCCACGTTCTGGGAACTGGCTGGAAGGGGCAAGAGGTCATGAGCCCCGCAGCCTGTGCC	GRCh38
NC_000009.11:g.139569402_139569403insTGGGCACCAGGTGCCCACGTTCTGGGAACTGGCTGGAAGGGGCAAGAGGTCATGAGCCCCGCAGCCTGTGCC , CM000671.1:g.139569402_139569403insTGGGCACCAGGTGCCCACGTTCTGGGAACTGGCTGGAAGGGGCAAGAGGTCATGAGCCCCGCAGCCTGTGCC	GRCh37
NC_000009.10:g.138689223_138689224insTGGGCACCAGGTGCCCACGTTCTGGGAACTGGCTGGAAGGGGCAAGAGGTCATGAGCCCCGCAGCCTGTGCC	NCBI36
NG_008090.1:g.17513_17514insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-140_589-139insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA MANE Select	ENSP00000360761.2:n.589-140_589-139insCAGGCTGCGGGGCTCATGACCTC...
ENST00000371694.7:c.493-140_493-139insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA	ENSP00000360759.3:n.493-140_493-139insCAGGCTGCGGGGCTCATGACCTC...
ENST00000371696.6:c.589-140_589-139insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA	ENSP00000360761.2:n.589-140_589-139insCAGGCTGCGGGGCTCATGACCTC...
ENST00000472820.1:n.517-140_517-139insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA
ENST00000538402.1:c.589-140_589-139insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA	ENSP00000438919.1:n.589-140_589-139insCAGGCTGCGGGGCTCATGACCTC...
NM_001012727.1:c.493-140_493-139insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA	NP_001012745.1:n.493-140_493-139insCAGGCTGCGGGGCTCATGACCTCTTG...
NM_006412.3:c.589-140_589-139insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA	NP_006403.2:n.589-140_589-139insCAGGCTGCGGGGCTCATGACCTCTTGCCC...
NM_006412.4:c.589-140_589-139insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA MANE Select	NP_006403.2:n.589-140_589-139insCAGGCTGCGGGGCTCATGACCTCTTGCCC...
NM_001012727.2:c.493-140_493-139insCAGGCTGCGGGGCTCATGACCTCTTGCCCCTTCCAGCCAGTTCCCAGAACGTGGGCACCTGGTGCCCAGGCA	NP_001012745.1:n.493-140_493-139insCAGGCTGCGGGGCTCATGACCTCTTG...