Canonical Allele Identifier: CA2692653405
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673535-C-CGAGCCA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673540_136673541insAGAGCC , CM000671.2:g.136673540_136673541insAGAGCC GRCh38
NC_000009.11:g.139567992_139567993insAGAGCC , CM000671.1:g.139567992_139567993insAGAGCC GRCh37
NC_000009.10:g.138687813_138687814insAGAGCC NCBI36
NG_008090.1:g.18924_18925insTGGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*216_*217insTGGCTC MANE Select ENSP00000360761.2:n.*216_*217insTGGCTC
ENST00000371694.7:c.*216_*217insTGGCTC ENSP00000360759.3:n.*216_*217insTGGCTC
ENST00000371696.6:c.*216_*217insTGGCTC ENSP00000360761.2:n.*216_*217insTGGCTC
ENST00000538402.1:c.*216_*217insTGGCTC ENSP00000438919.1:n.*216_*217insTGGCTC
NM_001012727.1:c.*216_*217insTGGCTC NP_001012745.1:n.*216_*217insTGGCTC
NM_006412.3:c.*216_*217insTGGCTC NP_006403.2:n.*216_*217insTGGCTC
NM_006412.4:c.*216_*217insTGGCTC MANE Select NP_006403.2:n.*216_*217insTGGCTC
NM_001012727.2:c.*216_*217insTGGCTC NP_001012745.1:n.*216_*217insTGGCTC
Search 100 bp 5'
Search 100 bp 3'