Canonical Allele Identifier: CA2692654806
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136676914-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676917del , CM000671.2:g.136676917del GRCh38
NC_000009.11:g.139571369del , CM000671.1:g.139571369del GRCh37
NC_000009.10:g.138691190del NCBI36
NG_008090.1:g.15545del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.492+46del MANE Select ENSP00000360761.2:n.492+46del
ENST00000371694.7:c.492+46del ENSP00000360759.3:n.492+46del
ENST00000371696.6:c.492+46del ENSP00000360761.2:n.492+46del
ENST00000472820.1:n.420+46del
ENST00000538402.1:c.492+46del ENSP00000438919.1:n.492+46del
NM_001012727.1:c.492+46del NP_001012745.1:n.492+46del
NM_006412.3:c.492+46del NP_006403.2:n.492+46del
NM_006412.4:c.492+46del MANE Select NP_006403.2:n.492+46del
NM_001012727.2:c.492+46del NP_001012745.1:n.492+46del
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