Canonical Allele Identifier: CA2579519918
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136674726-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674731del , CM000671.2:g.136674731del GRCh38
NC_000009.11:g.139569183del , CM000671.1:g.139569183del GRCh37
NC_000009.10:g.138689004del NCBI36
NG_008090.1:g.17733del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.661+8del MANE Select ENSP00000360761.2:n.661+8del
ENST00000371694.7:c.565+8del ENSP00000360759.3:n.565+8del
ENST00000371696.6:c.661+8del ENSP00000360761.2:n.661+8del
ENST00000472820.1:n.589+8del
ENST00000538402.1:c.661+8del ENSP00000438919.1:n.661+8del
NM_001012727.1:c.565+8del NP_001012745.1:n.565+8del
NM_006412.3:c.661+8del NP_006403.2:n.661+8del
NM_006412.4:c.661+8del MANE Select NP_006403.2:n.661+8del
NM_001012727.2:c.565+8del NP_001012745.1:n.565+8del
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