Canonical Allele Identifier: CA591184518
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1335702321
gnomAD v2: 9-139571175-AC-A
gnomAD v4: 9-136676723-AC-A
MyVariant Identifiers: chr9:g.139571176del (hg19) chr9:g.136676724del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676727del , CM000671.2:g.136676727del GRCh38
NC_000009.11:g.139571179del , CM000671.1:g.139571179del GRCh37
NC_000009.10:g.138691000del NCBI36
NG_008090.1:g.15736del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.493-44del MANE Select ENSP00000360761.2:n.493-44del
ENST00000371694.7:c.492+237del ENSP00000360759.3:n.492+237del
ENST00000371696.6:c.493-44del ENSP00000360761.2:n.493-44del
ENST00000472820.1:n.421-44del
ENST00000538402.1:c.493-44del ENSP00000438919.1:n.493-44del
NM_001012727.1:c.492+237del NP_001012745.1:n.492+237del
NM_006412.3:c.493-44del NP_006403.2:n.493-44del
NM_006412.4:c.493-44del MANE Select NP_006403.2:n.493-44del
NM_001012727.2:c.492+237del NP_001012745.1:n.492+237del
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