Canonical Allele Identifier: CA2692654178
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136674702-GCCTACAC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674705_136674711del , CM000671.2:g.136674705_136674711del GRCh38
NC_000009.11:g.139569157_139569163del , CM000671.1:g.139569157_139569163del GRCh37
NC_000009.10:g.138688978_138688984del NCBI36
NG_008090.1:g.17751_17757del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.661+26_661+32del MANE Select ENSP00000360761.2:n.661+26_661+32del
ENST00000371694.7:c.565+26_565+32del ENSP00000360759.3:n.565+26_565+32del
ENST00000371696.6:c.661+26_661+32del ENSP00000360761.2:n.661+26_661+32del
ENST00000472820.1:n.589+26_589+32del
ENST00000538402.1:c.661+26_661+32del ENSP00000438919.1:n.661+26_661+32del
NM_001012727.1:c.565+26_565+32del NP_001012745.1:n.565+26_565+32del
NM_006412.3:c.661+26_661+32del NP_006403.2:n.661+26_661+32del
NM_006412.4:c.661+26_661+32del MANE Select NP_006403.2:n.661+26_661+32del
NM_001012727.2:c.565+26_565+32del NP_001012745.1:n.565+26_565+32del
Search 100 bp 5'
Search 100 bp 3'