Canonical Allele Identifier: CA861080341
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1289508912
gnomAD v4: 9-136673559-G-GC
MyVariant Identifiers: chr9:g.139568011_139568012insC (hg19) chr9:g.136673559_136673560insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673564dup , CM000671.2:g.136673564dup GRCh38
NC_000009.11:g.139568016dup , CM000671.1:g.139568016dup GRCh37
NC_000009.10:g.138687837dup NCBI36
NG_008090.1:g.18900dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*192dup MANE Select ENSP00000360761.2:n.*192dup
ENST00000371694.7:c.*192dup ENSP00000360759.3:n.*192dup
ENST00000371696.6:c.*192dup ENSP00000360761.2:n.*192dup
ENST00000538402.1:c.*192dup ENSP00000438919.1:n.*192dup
NM_001012727.1:c.*192dup NP_001012745.1:n.*192dup
NM_006412.3:c.*192dup NP_006403.2:n.*192dup
NM_006412.4:c.*192dup MANE Select NP_006403.2:n.*192dup
NM_001012727.2:c.*192dup NP_001012745.1:n.*192dup
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