Canonical Allele Identifier: CA2692654591
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136676635-C-CCCCATTGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676637_136676644dup , CM000671.2:g.136676637_136676644dup GRCh38
NC_000009.11:g.139571089_139571096dup , CM000671.1:g.139571089_139571096dup GRCh37
NC_000009.10:g.138690910_138690917dup NCBI36
NG_008090.1:g.15817_15824dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.530_537dup MANE Select ENSP00000360761.2:p.Asp180ThrfsTer?
ENST00000371694.7:c.492+318_492+325dup ENSP00000360759.3:n.492+318_492+325dup
ENST00000371696.6:c.530_537dup ENSP00000360761.2:p.Asp180ThrfsTer?
ENST00000472820.1:n.458_465dup
ENST00000538402.1:c.530_537dup ENSP00000438919.1:p.Asp180ThrfsTer?
NM_001012727.1:c.492+318_492+325dup NP_001012745.1:n.492+318_492+325dup
NM_006412.3:c.530_537dup NP_006403.2:p.Asp180ThrfsTer?
NM_006412.4:c.530_537dup MANE Select NP_006403.2:p.Asp180ThrfsTer?
NM_001012727.2:c.492+318_492+325dup NP_001012745.1:n.492+318_492+325dup
Search 100 bp 5'
Search 100 bp 3'